Clinical, biochemical and genetic characteristics and long-term follow-up of five patients with malonyl-CoA decarboxylase deficiency-Reference-Cited by-同舟云学术

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Clinical, biochemical and genetic characteristics and long-term follow-up of five patients with malonyl-CoA decarboxylase deficiency

Published:2024-10 Issue:9 Volume:46 Page:286-293
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Zhang J.M.,Hao L.L.,Qiu W.J.,Zhang H.W.,Chen T.,Ji W.J.,Zhang Y.,Liu F.,Gu X.F.,Yang S.H.,Han L.S.

Publisher

Elsevier BV

Reference32 articles.

1. Malonyl coenzyme A decarboxylase deficiency;Brown;J Inherit Metab Dis,1984

2. Cloning and mutational analysis of human malonyl-coenzyme A decarboxylase;Gao;J Lipid Res,1999

3. Impaired mitochondrial fatty acid oxidative flux in fibroblasts from a patient with malonyl-CoA decarboxylase deficiency;Bennett;Mol Genet Metab,2001

4. The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis;McGarry;Eur J Biochem,1997

5. Malonyl-CoA decarboxylase deficiency: long-term follow-up of a patient new clinical features and novel mutations;Polinati;Brain Dev,2015

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