Clinical, biochemical, and mutational spectrum of peroxisomal acyl–coenzyme A oxidase deficiency-Reference-Cited by-同舟云学术

Clinical, biochemical, and mutational spectrum of peroxisomal acyl–coenzyme A oxidase deficiency

Published:2007 Issue:9 Volume:28 Page:904-912
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Ferdinandusse Sacha,Denis Simone,Hogenhout Eveline M.,Koster Janet,van Roermund Carlo W.T.,IJlst Lodewijk,Moser Ann B.,Wanders Ronald J.A.,Waterham Hans R.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. Regulation of differentially spliced transcripts of acyl-CoA oxidase in the rat

2. Identification of the peroxisomal β-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid

3. Evidence for increased oxidative stress in peroxisomal D-bifunctional protein deficiency

4. Clinical and biochemical spectrum of D-bifunctional protein deficiency

5. Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy.

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