2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency Is Caused by Mutations in the HADH2 Gene-Reference-Cited by-同舟云学术

2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency Is Caused by Mutations in the HADH2 Gene

Published:2003-05 Issue:5 Volume:72 Page:1300-1307
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ofman Rob,Jos Ruiter P.N.,Feenstra Marike,Duran Marinus,Bwee Poll-The Tien,Zschocke Johannes,Ensenauer Regina,Lehnert Willy,Sass Jörn Oliver,Sperl Wolfgang,Ronald Wanders J.A.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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5. Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals;Ghaedi;Exp Cell Res,1999

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