Broad phenotypic variability in patients with complex I deficiency due to mutations in NDUFS1 and NDUFV1-Reference-Cited by-同舟云学术

Broad phenotypic variability in patients with complex I deficiency due to mutations in NDUFS1 and NDUFV1

Published:2015-03 Issue: Volume:21 Page:33-40
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Björkman Kristoffer,Sofou Kalliopi,Darin Niklas,Holme Elisabeth,Kollberg Gittan,Asin-Cayuela Jorge,Holmberg Dahle Karin M.,Oldfors Anders,Moslemi Ali-Reza,Tulinius Már

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference41 articles.

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3. Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophic cardiomyopathy and encephalopathy;Benit;Hum. Mutat.,2003

4. Energy converting NADH:quinone oxidoreductase (complex I);Brandt;Annu. Rev. Biochem.,2006

5. Siblings with leukoencephalopathy;Breningstall;Semin. Pediatr. Neurol.,2008

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