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Meixia Yuan

Wenzhou Medical College

5

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132

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Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.

2010 Molecular Genetics and Metabolism
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Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.

2010 Biochimica et Biophysica Acta
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Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families.

2010 Biochemical and Biophysical Research Communications
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The Influence of Secondary Mutations of Mitochondrial DNA on Leber's Hereditary Optic Neuropathy

2009
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Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation

2009 Biochemical and Biophysical Research Communications
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