A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) gene-Reference-Cited by-同舟云学术

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A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) gene

Published:1993 Issue:4 Volume:2 Page:488-488
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Andresen Brage S.,Kølvraa Steen,Bross Peter,Bolund Lars,Curtis Diana,Eiberg Hans,Zhang Zhifang,Kelly Daniel P.,Strauss Arnold W.,Gregersen Niels

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/2/4/488/2232269/2-4-488.pdf

Cited by 10 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. A synonymous polymorphic variation in ACADM exon 11 affects splicing efficiency and may affect fatty acid oxidation;Molecular Genetics and Metabolism;2013-09

2. Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: Under-representation of the common c.985 A > G mutation in the New York state population;American Journal of Medical Genetics Part A;2008

3. Rapid, comprehensive screening of the human medium chain acyl-CoA dehydrogenase gene;Molecular Genetics and Metabolism;2004-06

4. Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutations Identified by MS/MS-Based Prospective Screening of Newborns Differ from Those Observed in Patients with Clinical Symptoms: Identification and Characterization of a New, Prevalent Mutation That Results in Mild MCAD Deficiency*;The American Journal of Human Genetics;2001-06

5. The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype?;Human Molecular Genetics;1997-05-01

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