Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency-Reference-Cited by-同舟云学术

Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency

Published:2010-06-22 Issue:8 Volume:31 Page:930-941
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Morán María,Marín-Buera Lorena,Gil-Borlado M. Carmen,Rivera Henry,Blázquez Alberto,Seneca Sara,Vázquez-López María,Arenas Joaquín,Martín Miguel A.,Ugalde Cristina

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21294/fullpdf

Reference37 articles.

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3. Ultrastructure of the mitochondrion and its bearing on function and bioenergetics;Benard;Antioxid Redox Signal,2008

4. Respiratory-chain diseases related to complex III deficiency;Benit;Biochim Biophys Acta,2009

5. Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient;Blazquez;Neuromuscul Disord,2009

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