載入...

Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism.

The presence or absence of a recently observed mitochondrial DNA (mtDNA) mutation associated with Leber hereditary optic neuroretinopathy (LHON) was tested in 19 Finnish families with cases of LHON. Leukocyte and muscle DNA from individuals with optic atrophy, microangiopathy, or normal fundi from m...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Vilkki, J, Savontaus, M L, Nikoskelainen, E K
格式: Artigo
語言:Inglês
出版: 1989
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683352/
https://ncbi.nlm.nih.gov/pubmed/2757028
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!