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TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

✍ Scribed by Čížková, Alena; Stránecký, Viktor; Mayr, Johannes A; Tesařová, Markéta; Havlíčková, Vendula; Paul, Jan; Ivánek, Robert; Kuss, Andreas W; Hansíková, Hana; Kaplanová, Vilma

Book ID: 109914335
Publisher: Nature Publishing Group
Year: 2008
Tongue: English
Weight: 362 KB
Volume: 40
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng.246

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