Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency-Reference-Cited by-同舟云学术

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Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency

Published:2012-05-18 Issue:15 Volume:21 Page:3435-3448
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Cornelius N.,Frerman F. E.,Corydon T. J.,Palmfeldt J.,Bross P.,Gregersen N.,Olsen R. K. J.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference58 articles.

1. Acyl-CoA dehydrogenases. A mechanistic overview

2. Clear relationship betweenETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency

3. Late-onset form of β-electron transfer flavoprotein deficiency

4. Molecular study of electron transfer flavoprotein α-subunit deficiency in two Japanese children with different phenotypes of glutaric acidemia type II

5. Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency

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