Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.20456/fullpdf
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5. A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
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