Fatal infantile mitochondrial encephalomyopathy,...

Journal of Medical Genetics 2016 / 02 Vol. 53; Iss. 2

Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation

Spiegel, Ronen, Saada, Ann, Flannery, Padraig J, Burté, Florence, Soiferman, Devorah, Khayat, Morad, Eisner, Verónica, Vladovski, Eugene, Taylor, Robert W, Bindoff, Laurence A, Shaag, Avraham, Mandel,
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Volume:
53
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2015-103361
Date:
February, 2016
File:
PDF, 570 KB
english, 2016
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