Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects-Reference-Cited by-同舟云学术

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Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects

Published:2000-01 Issue:9201 Volume:355 Page:389-394
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Leonard JV,Schapira AHV

Publisher

Elsevier BV

Subject

General Medicine

Reference64 articles.

1. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency;Bourgeron;Nature Genet,1995

2. Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit;Van den Heuvel;Am J Hum Genet,1998

3. The first nuclear-encoded complex I mutation in a patient with Leigh syndrome;Loeffen;Am J Hum Genet,1998

4. Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I;Triepels;Ann Neurol,1999

5. Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy;Schuelke;Nat Genet,1999

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