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pro vyhledávání: '"Magdalena Korwin-Rujna"'
Autor:
Katarzyna Tońska, Jerzy Szaflik, Anna M. Ambroziak, Jacek P. Szaflik, Magdalena Korwin-Rujna, Marzena Kurzawa, Ewa Bartnik, Ewa Grabowska
Publikováno v:
Mitochondrion. 8(5-6)
Three mutations in mitochondrial DNA complex I genes are responsible for over 90% of Leber hereditary optic neuropathy (LHON) cases in Europe. A family with two LHON mutations--practically homoplasmic 11778G>A and varying levels of 3460G>A--was found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5608ed9b379b8850028e172c3ee380ea
https://pubmed.ncbi.nlm.nih.gov/18801464
https://pubmed.ncbi.nlm.nih.gov/18801464
