Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene
Leber's hereditary optic neuropathy (LHON) is a maternally inherited form of retinal ganglion cell degeneration leading to optic atrophy in young adults. Several mutations in different genes can cause LHON (heterogeneity). The ND6 gene is one of the mitochondrial genes that encodes subunit 6 of...
Main Authors: | M. Houshmand, T. Mahmoudi, M. Shafa Shariat Panahi, Y. Seyedena, S. Saber, M. Ataei |
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Format: | Article |
Language: | English |
Published: |
Associação Brasileira de Divulgação Científica
2006-06-01
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Series: | Brazilian Journal of Medical and Biological Research |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2006000600004 |
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