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	201.	Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations. [electronic resource] by Brown, M D Allen, J C Van Stavern, G P Newman, N J Wallace, D C Producer: 20020123 In: American journal of medical genetics vol. 104 Availability: No items available. Save to lists Add to cart (remove)
	202.	Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. [electronic resource] by Shoffner, J M Lott, M T Lezza, A M Seibel, P Ballinger, S W Wallace, D C Producer: 19900718 In: Cell vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	203.	Fast capillary electrophoresis-laser induced fluorescence analysis of ligase chain reaction products: human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy. [electronic resource] by Muth, J Williams, P M Williams, S J Brown, M D Wallace, D C Karger, B L Producer: 19970902 In: Electrophoresis vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	204.	Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy. [electronic resource] by Torroni, A Carelli, V Petrozzi, M Terracina, M Barboni, P Malpassi, P Wallace, D C Scozzari, R Producer: 19960801 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	205.	A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator. [electronic resource] by Graham, B H Waymire, K G Cottrell, B Trounce, I A MacGregor, G R Wallace, D C Producer: 19970729 In: Nature genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	206.	Mitochondrial DNA and Y chromosome-specific polymorphisms in the Seminole Tribe of Florida. [electronic resource] by Huoponen, K Torroni, A Wickman, P R Sellitto, D Gurley, D S Scozzari, R Wallace, D C Producer: 19970722 In: European journal of human genetics : EJHG vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	207.	Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. [electronic resource] by Brown, M D Voljavec, A S Lott, M T Torroni, A Yang, C C Wallace, D C Producer: 19920225 In: Genetics vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	208.	Computer prediction of peptide maps: assignment of polypeptides to human and mouse mitochondrial DNA genes by analysis of two-dimensional-proteolytic digest gels. [electronic resource] by Wallace, D C Yang, J H Ye, J H Lott, M T Oliver, N A McCarthy, J Producer: 19860620 In: American journal of human genetics vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	209.	Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction. [electronic resource] by Wallace, D C Lott, M T Lezza, A M Seibel, P Voljavec, A S Shoffner, J M Producer: 19910124 In: Pediatric research vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	210.	Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude. [electronic resource] by Torroni, A Miller, J A Moore, L G Zamudio, S Zhuang, J Droma, T Wallace, D C Producer: 19940502 In: American journal of physical anthropology vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	211.	Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team. [electronic resource] by Newman, N J Torroni, A Brown, M D Lott, M T Fernandez, M M Wallace, D C Producer: 19940906 In: American journal of ophthalmology vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	212.	Atypical Leber's hereditary optic neuropathy with molecular confirmation. [electronic resource] by Weiner, N C Newman, N J Lessell, S Johns, D R Lott, M T Wallace, D C Producer: 19930609 In: Archives of neurology vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	213.	Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations. [electronic resource] by Wallace, D C Ye, J H Neckelmann, S N Singh, G Webster, K A Greenberg, B D Producer: 19880617 In: Current genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	214.	Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age. [electronic resource] by Corral-Debrinski, M Horton, T Lott, M T Shoffner, J M Beal, M F Wallace, D C Producer: 19930623 In: Nature genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	215.	DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene. [electronic resource] by Pratt, V M Jackson, C E Wallace, D C Gurley, D S Feit, A Feldman, G L Producer: 19970826 In: American journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	216.	Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene. [electronic resource] by Esposito, L A Kokoszka, J E Waymire, K G Cottrell, B MacGregor, G R Wallace, D C Producer: 20000525 In: Free radical biology & medicine vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	217.	Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation. [electronic resource] by Stone, E M Newman, N J Miller, N R Johns, D R Lott, M T Wallace, D C Producer: 19920507 In: Journal of clinical neuro-ophthalmology vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	218.	Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy. [electronic resource] by Shoffner, J M Lott, M T Voljavec, A S Soueidan, S A Costigan, D A Wallace, D C Producer: 19891201 In: Proceedings of the National Academy of Sciences of the United States of America vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	219.	Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutation. [electronic resource] by Ortiz, R G Newman, N J Shoffner, J M Kaufman, A E Koontz, D A Wallace, D C Producer: 19931207 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	220.	De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy. [electronic resource] by Biousse, V Brown, M D Newman, N J Allen, J C Rosenfeld, J Meola, G Wallace, D C Producer: 19971114 In: Neurology vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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