Author:
Mahoui S.,Belkhamsa O.,Ait Kaci I.,Abada Bendib M.,Castelnovo G.
Subject
Clinical Neurology,Neurology
Reference5 articles.
1. Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia;Jun;Mol Cell Biol,1996
2. Pediatric-onset dystonia associated with bilateral striatal necrosis and G14459A mutation in a Korean family: a case report;Park,2010
3. Bilateral striatal necrosis caused by a founder mitochondrial 14459G N A mutation in two independent Japanese families;Hirayanagi;J Neurol Sci,2017
4. Maladie de Leber « Plus » : neuropathie optique, syndrome parkinsonien et ophtalmoplégie supranucléaire;Thobois;Rev Neurol,1997
5. Childhood-onset progressive dystonia with mitochondrial DNA G14459A mutation: efficacy of long-term sodium succinate treatment;Koide,2014
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