Late-onset form of β-electron transfer flavoprotein deficiency-Reference-Cited by-同舟云学术

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Late-onset form of β-electron transfer flavoprotein deficiency

Published:2003-04 Issue:4 Volume:78 Page:247-249
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Curcoy A.,Olsen R.K.J.,Ribes A.,Trenchs V.,Vilaseca M.A.,Campistol J.,Osorio J.H.,Andresen B.S.,Gregersen N.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference15 articles.

1. Multiple acyl-coenzyme A dehydrogenation disorder responsive to riboflavin: substrate oxidation, flavin metabolism, and flavoenzyme activities in fibroblasts;Rhead;Pediatr. Res.,1993

2. Riboflavin theraphy. Biochemical heterogeneity in two adult lipid storage myopathies;Vergani;Brain,1999

3. Rivoflavin-responsive defects of β-oxidation;Gregersen;J. Inher. Metab. Dis.,1985

4. Defects of electron transfer flavoprotein and electron transfer falvoprotein ubiquinone oxidoreductase: glutaric acidemia type II;Frerman,2000

5. Newly identified forms of electron transfer flavoprotein deficiency in two patients with glutaric aciduria type II;Yamaguchi;Pediatr. Res.,1991

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