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	2881.	Expansion of polyglutamine repeat in huntingtin leads to abnormal protein interactions involving calmodulin. [electronic resource] by Bao, J Sharp, A H Wagster, M V Becher, M Schilling, G Ross, C A Dawson, V L Dawson, T M Producer: 19960718 In: Proceedings of the National Academy of Sciences of the United States of America vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2882.	Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorder. [electronic resource] by Rubinsztein, D C Leggo, J Crow, T J DeLisi, L E Walsh, C Jain, S Paykel, E S Producer: 19970123 In: American journal of medical genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2883.	X chromosome inactivation pattern in female carriers of X linked hypophosphataemic rickets. [electronic resource] by Orstavik, K H Orstavik, R E Halse, J Knudtzon, J Producer: 19961227 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2884.	A family of dispersed DNA elements that contain GAA repeats in Toxoplasma gondii. [electronic resource] by Messina, M Kim, S Sibley, L D Producer: 19970303 In: Molecular and biochemical parasitology vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2885.	Apparent FMR1 allele instability in non-fragile X males. [electronic resource] by Brown, W T Nolin, S L Producer: 20010201 In: Genetic testing vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2886.	Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1. [electronic resource] by Mikami, M Yasuda, T Terao, A Nakamura, M Ueno, S Tanabe, H Tanaka, T Onuma, T Goto, Y Kaneko, S Sano, A Producer: 19991004 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2887.	Characterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI). [electronic resource] by Bardien-Kruger, Soraya Wulff, Heike Arieff, Zainu Brink, Paul Chandy, K George Corfield, Valerie Producer: 20020723 In: European journal of human genetics : EJHG vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2888.	Mitochondrial dysfunction in Friedreich's ataxia: from pathogenesis to treatment perspectives. [electronic resource] by Lodi, R Rajagopalan, B Bradley, J L Taylor, D J Crilley, J G Hart, P E Blamire, A M Manners, D Styles, P Schapira, A H V Cooper, J M Producer: 20021028 In: Free radical research vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2889.	Parameter-based assessment of spatial and non-spatial attentional deficits in Huntington's disease. [electronic resource] by Finke, Kathrin Bublak, Peter Dose, Matthias Müller, Hermann J Schneider, Werner X Producer: 20060531 In: Brain : a journal of neurology vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2890.	Double-strand breaks in the myotonic dystrophy type 1 and the fragile X syndrome triplet repeat sequences induce different types of mutations in DNA flanking sequences in Escherichia coli. [electronic resource] by Kosmider, Beata Wells, Robert D Producer: 20061220 In: Nucleic acids research vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2891.	[Cloning and characterization of a novel trinucleotide repeat-containing gene GARP from Euplotes octocarinatus]. [electronic resource] by Xu, Jing Wang, Wei Chai, Bao-Feng Liang, Ai-Hua Producer: 20090327 In: Yi chuan = Hereditas vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2892.	Genome-wide linkage survey for genetic loci that affect the risk of suicide attempts in families with recurrent, early-onset, major depression. [electronic resource] by Zubenko, George S Maher, Brion S Hughes, Hugh B Zubenko, Wendy N Scott Stiffler, J Marazita, Mary L Producer: 20050216 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 129B Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2893.	SCA3: neurological features, pathogenesis and animal models. [electronic resource] by Riess, Olaf Rüb, Udo Pastore, Annalisa Bauer, Peter Schöls, Ludger Producer: 20090515 In: Cerebellum (London, England) vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2894.	A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment. [electronic resource] by Price, Maureen G Yoo, Jong W Burgess, Daniel L Deng, Fang Hrachovy, Richard A Frost, James D Noebels, Jeffrey L Producer: 20090803 In: The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2895.	Prevention of depressive behaviour in the YAC128 mouse model of Huntington disease by mutation at residue 586 of huntingtin. [electronic resource] by Pouladi, Mahmoud A Graham, Rona K Karasinska, Joanna M Xie, Yuanyun Santos, Rachelle Dar Petersén, Asa Hayden, Michael R Producer: 20091001 In: Brain : a journal of neurology vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2896.	Trinucleotide repeats of programmed cell death-1 gene are associated with susceptibility to type 1 diabetes mellitus. [electronic resource] by Hiromine, Yoshihisa Ikegami, Hiroshi Fujisawa, Tomomi Nojima, Koji Kawabata, Yumiko Noso, Shinsuke Asano, Katsuaki Fukai, Aya Ogihara, Toshio Producer: 20070821 In: Metabolism: clinical and experimental vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2897.	Distribution of CTG repeats at the DMPK gene in myotonic dystrophy patients and healthy individuals from the Mexican population. [electronic resource] by Magaña, J J Cortés-Reynosa, P Escobar-Cedillo, R Gómez, R Leyva-García, N Cisneros, B Producer: 20110526 In: Molecular biology reports vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2898.	Clinical profile, BRCA2 expression, and the androgen receptor CAG repeat region in Egyptian and Moroccan male breast cancer patients. [electronic resource] by Gilbert, Samuel F Soliman, Amr S Karkouri, Mehdi Quinlan-Davidson, Meaghen Strahley, Ashley Eissa, Mohab Dey, Subhojit Hablas, Ahmed Seifeldin, Ibrahim A Ramadan, Mohamed Benjaafar, Noureddine Toy, Kathy Merajver, Sofia D Producer: 20120625 In: Breast disease vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2899.	[Analysis of SCA3/MJD3 gene mutation and genetic polymorphism in a guangxi family with spinocerebellar ataxia 3]. [electronic resource] by Chang, Rong-Ni Yuan, Guang-Zhi Tan, Jian-Qiang Lai, Qing-Niao Ma, Jun Yang, Yi-Jin Shu, Wei Hou, Wei Yuan, Zhi-Gang Producer: 20140401 In: Yi chuan = Hereditas vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2900.	Neurobehavioral deficits in the KIKO mouse model of Friedreich's ataxia. [electronic resource] by McMackin, Marissa Z Henderson, Chelsea K Cortopassi, Gino A Producer: 20171124 In: Behavioural brain research vol. 316 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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