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	1.	No MELAS syndrome without heteroplasmy levels or multisystem examination. [electronic resource] by Finsterer, J Maeztu, C Producer: 20210908 In: Neurologia vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel heteroplasmic mutation in mitochondrial tRNA [electronic resource] by Heidari, Mohammad Mehdi Keshmirshekan, Abolfazl Bidakhavidi, Mozhgan Khosravi, Azam Bandari, Zeinab Khatami, Mehri Nafissi, Shahriar Producer: 20210318 In: Acta neurologica Belgica vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel homoplasmic mitochondrial DNA mutation (m.13376T>C, p.I347T) of MELAS presenting characteristic medial temporal lobe atrophy. [electronic resource] by Sasaki, Ryo Ohta, Yasuyuki Hatanaka, Noriko Tadokoro, Koh Nomura, Emi Shang, Jingwei Takemoto, Mami Hishikawa, Nozomi Yamashita, Toru Omote, Yoshio Morimoto, Eisaku Teshigawara, Sanae Wada, Jun Goto, Yu-Ichi Abe, Koji Producer: 20210319 In: Journal of the neurological sciences vol. 408 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mitochondrial DNA heteroplasmy in disease and targeted nuclease-based therapeutic approaches. [electronic resource] by Nissanka, Nadee Moraes, Carlos T Producer: 20210427 In: EMBO reports vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Unprecedented Intraindividual Structural Heteroplasmy in Eleocharis (Cyperaceae, Poales) Plastomes. [electronic resource] by Lee, Chaehee Ruhlman, Tracey A Jansen, Robert K Producer: 20210713 In: Genome biology and evolution vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	DNA-editing enzymes as potential treatments for heteroplasmic mtDNA diseases. [electronic resource] by Zekonyte, U Bacman, S R Moraes, C T Producer: 20201217 In: Journal of internal medicine vol. 287 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Characterization of background noise in MiSeq MPS data when sequencing human mitochondrial DNA from various sample sources and library preparation methods. [electronic resource] by McElhoe, Jennifer A Holland, Mitchell M Producer: 20210607 In: Mitochondrion vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Homoplasmy of the Mitochondrial DNA Mutation m.616T>C Leads to Mitochondrial Tubulointerstitial Kidney Disease and Encephalopathia. [electronic resource] by Lorenz, Robin Ahting, Uwe Betzler, Cornelia Heimering, Sigrid Borggräfe, Ingo Lange-Sperandio, Bärbel Producer: 20210308 In: Nephron vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Impact of the sequencing method on the detection and interpretation of mitochondrial DNA length heteroplasmy. [electronic resource] by Sturk-Andreaggi, Kimberly Parson, Walther Allen, Marie Marshall, Charla Producer: 20210308 In: Forensic science international. Genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Comparison of whole mitochondrial genome variants between hair shafts and reference samples using massively parallel sequencing. [electronic resource] by Kim, Bo Min Hong, Sae Rom Chun, Hein Kim, Sangwoo Shin, Kyoung-Jin Producer: 20210201 In: International journal of legal medicine vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	The execution of the Romanov family at Yekatarinberg. [electronic resource] by Byard, Roger W Producer: 20210406 In: Forensic science, medicine, and pathology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Sensitivity of mitochondrial DNA heteroplasmy detection using Next Generation Sequencing. [electronic resource] by González, María Del Mar Ramos, Amanda Aluja, Maria Pilar Santos, Cristina Producer: 20210223 In: Mitochondrion vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Three rare pathogenic mtDNA substitutions in LHON patients with low heteroplasmy. [electronic resource] by Krylova, Tatiana D Sheremet, Natalia L Tabakov, Vyacheslav Yu Lyamzaev, Konstantin G Itkis, Yulia S Tsygankova, Polina G Andreeva, Natalia A Shmelkova, Maria S Nevinitsyna, Tatiana A Kadyshev, Vitaly V Zakharova, Ekaterina Yu Producer: 20210223 In: Mitochondrion vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Manipulation of mitochondrial genes and mtDNA heteroplasmy. [electronic resource] by Bacman, Sandra R Gammage, P A Minczuk, M Moraes, Carlos T Producer: 20201224 In: Methods in cell biology vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Heteroplasmy and phenotype spectrum of the mitochondrial tRNA [electronic resource] by Liu, Gailing Shen, Xiya Sun, Yongan Lv, Qing Li, Yuanyuan Du, Ailian Producer: 20210319 In: Journal of the neurological sciences vol. 408 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Detection of mitochondrial DNA variants at low level heteroplasmy in pediatric CNS and extra-CNS solid tumors with three different enrichment methods. [electronic resource] by Kaneva, Kristiyana Merkurjev, Daria Ostrow, Dejerianne Ryutov, Alex Triska, Petr Stachelek, Kevin Cobrinik, David Biegel, Jaclyn A Gai, Xiaowu Producer: 20210223 In: Mitochondrion vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Role of mitochondrial DNA variants in the development of fragile X-associated tremor/ataxia syndrome. [electronic resource] by Alvarez-Mora, Maria Isabel Santos, Cristina Carreño-Gago, Lidia Madrigal, Irene Tejada, Maria Isabel Martinez, Francisco Izquierdo-Alvarez, Silvia Garcia-Arumi, Elena Mila, Montserrat Rodriguez-Revenga, Laia Producer: 20210607 In: Mitochondrion vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Associations of Peripheral Artery Disease With Calf Skeletal Muscle Mitochondrial DNA Heteroplasmy. [electronic resource] by Gonzalez-Freire, Marta Moore, A Zenobia Peterson, Charlotte A Kosmac, Kate McDermott, Mary M Sufit, Robert L Guralnik, Jack M Polonsky, Tamar Tian, Lu Kibbe, Melina R Criqui, Michael H Li, Lingyu Leeuwenburgh, Christian Ferrucci, Luigi Producer: 20210308 In: Journal of the American Heart Association vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)