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)

Author： Rezvani Zahra   Didari Elmira   Arastehkani Ahoura   Ghodsinejad Vadieh   Aryani Omid   Kamalidehghan Behnam   Houshmand Massoud  

Publisher： Springer Publishing Company

ISSN： 0301-4851

Source： Molecular Biology Reports, Vol.40, Iss.12, 2013-12, pp. : 6837-6841

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