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Scholar Results 1 - 1 of 1 citing Abu-Amero: Complex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation. (0.08 sec) 

A MELAS-associated ND1 mutation causing Leber hereditary optic neuropathy and spastic …


L Spruijt, HJ Smeets, A Hendrickx, MW … - Archives of neurology, 2007 - Am Med Assoc
Design Leber hereditary optic neuropathy is a mitochondrial disorder
characterized by isolated central visual loss. Of patients with LHON, 95% carry
a mutation in 1 of 3 mitochondrial DNA–encoded complex I genes. The ...
Cited by 6 - Related articles - BL Direct - All 6 versions


 


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