Clinical and diagnostic characteristics of complex III deficiency due to mutations in theBCS1Lgene-Reference-Cited by-同舟云学术

Clinical and diagnostic characteristics of complex III deficiency due to mutations in theBCS1Lgene

Published:2003-04-09 Issue:2 Volume:121A Page:126-131
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

De Meirleir Linda,Seneca Sara,Damis Eliane,Sepulchre Brigitte,Hoorens Anne,Gerlo Erik,García Silva M. Teres,Hernandez Elena Martín,Lissens Willy,Van Coster Rudy

Funder

Fund for Scientific Research Flanders (FWO Vlaanderen)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference30 articles.

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5. Bcs1p, an AAA-family member, is a chaperone for the assembly of the cytochrome bc(1) complex;Cruciat;EMBO J,1999

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