Malonyl CoA decarboxylase deficiency: C to T transition in intron 2 of the MCD gene-Reference-Cited by-同舟云学术

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Malonyl CoA decarboxylase deficiency: C to T transition in intron 2 of the MCD gene

Published:2001 Issue:6 Volume:65 Page:591-594
ISSN:0360-4012
Container-title:Journal of Neuroscience Research
language:en
Short-container-title:J. Neurosci. Res.

Author:

Surendran Sankar,Sacksteder Katherine A.,Gould Stephen J.,Coldwell James G.,Rady Peter L.,Tyring Stephan K.,Matalon Reuben

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience

Reference21 articles.

1. IIlegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuria

2. Ovalbumin gene: evidence for a leader sequence in mRNA and DNA sequences at the exon-intron boundaries.

3. Malonyl coenzyme a decarboxylase deficiency

4. Lipid biosynthesis in the sebaceous glands. Synthesis of multibranched fatty acids from methylmalonyl-coenzyme A in cell-free preparations from the uropygial gland of goose

5. Fatal neonatal malonic aciduria

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case report: A novel 5'-UTR-exon1-intron1 deletion in MLYCD in an IVF child with malonyl coenzyme A decarboxylase deficiency and literature review;Frontiers in Medicine;2023-05-03

2. A case of malonyl coenzyme A decarboxylase deficiency with novel mutations and literature review;Frontiers in Pediatrics;2023-04-17

3. Novel trifluoroacetophenone derivatives as malonyl-CoA decarboxylase inhibitors;Bioorganic & Medicinal Chemistry Letters;2007-02

4. Congenital and Acquired Heart Disease;Post-Genomic Cardiology;2007

5. Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiency;Journal of Inherited Metabolic Disease;2006-12-20

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