Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.

Kearns-Sayre syndrome (KSS) is a progressive neuromuscular disease characterised by ophtalmoplegia, cardiac bloc branch, pigmentary retinopathy associated with abnormal mitochondrial function. We have studied the mitochondrial DNA organization of patients presenting KSS and have found large deletion...

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Detalhes bibliográficos
Main Authors: Nelson, I, Degoul, F, Obermaier-Kusser, B, Romero, N, Borrone, C, Marsac, C, Vayssiere, J L, Gerbitz, K, Fardeau, M, Ponsot, G
Formato: Artigo
Idioma:Inglês
Publicado em: 1989
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC334951/
https://ncbi.nlm.nih.gov/pubmed/2813058
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