Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation-Reference-Cited by-同舟云学术

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Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation

Published:2003-10 Issue:7 Volume:26 Page:659
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Gargus J. J.¹,Boyle K.²,Bocian M.²,Roe D. S.³,Vianey-Saban C.⁴,Roe C. R.³

Affiliation:

1. ; Department of Physiology and Biophysics; University of California; Irvine California

2. ; Division of Human Genetics, Department of Pediatrics; University of California; Irvine California

3. ; Institute of Metabolic Disease; Baylor University Medical Center; Dallas Texas USA

4. ; Service de Biochimie Pédiatrique; Hôpital Debrousse; Lyon France

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/B:BOLI.0000005659.52200.c1/fullpdf

Reference26 articles.

1. Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activity;Arpa;Acta Neurol Scand,1994

2. Secondary inhibition of multiple NAD-requiring dehydrogenases in respiratory chain complex I deficiency: possible metabolic markers for the primary defect;Bennett;J Inherit Metab Dis,1993

3. Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts;Bertrand;Clin Chim Acta,1992

4. Hair and skin disorders as signs of mitochondrial disease;Bodemer;Pediatrics,1999

5. Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathy;Brown-Harrison;Biochem Mol Med,1996

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