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See Latest ArticlesMitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese
Biochemical and Biophysical Research Communications, 07/20/09
Zhang AM et al. – Protein secondary–structure modeling for the MT–ND1 protein harboring amino acid change S110N indicates that mutant m.3635G>A decreases the protein hydrophobicity. The current observations provide further support for a pathogenic role of m.3635G>A in patients with LHON.
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