Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene-Reference-Cited by-同舟云学术

Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene

Published:2003-10-23 Issue:5 Volume:54 Page:665-669
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Ugalde Cristina,Triepels Ralf H.,Coenen Marieke J.H.,Van Den Heuvel Lambert P.,Smeets Roel,Uusimaa Johanna,Briones Paz,Campistol Jaume,Majamaa Kari,Smeitink Jan A.M.,Nijtmans Leo G.J.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference20 articles.

1. The genetics and pathology of oxidative phosphorylation

2. Analysis of the Subunit Composition of Complex I from Bovine Heart Mitochondria*S

3. Leber hereditary optic neuropathy

4. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy

5. Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy

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