ArticleMolecular biology reports2013

Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON).

Zahra Rezvani et al.PubMed ↗Publisher ↗

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