Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations.
作者信息
Hofmann S, Bezold R, Jaksch M, Kaufhold P, Obermaier-Kusser B, Gerbitz K D
出版信息
Am J Hum Genet. 1997 Jun;60(6):1539-42. doi: 10.1016/S0002-9297(07)64248-7.
Abstract
摘要
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Genomics. 1997 Jan 1;39(1):8-18. doi: 10.1006/geno.1996.4474.
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Classification of European mtDNAs from an analysis of three European populations.通过对三个欧洲人群的分析对欧洲线粒体DNA进行分类。
Genetics. 1996 Dec;144(4):1835-50. doi: 10.1093/genetics/144.4.1835.
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Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.沃夫勒姆综合征与染色体4p16.1的连锁关系及遗传异质性证据。
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Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.莱伯遗传性视神经病变：线粒体细胞色素b基因突变的病因学作用
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