Author:
McKinney J.T,Longo N,Hahn S.H,Matern D,Rinaldo P,Strauss A.W,Dobrowolski S.F
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference29 articles.
1. Fatty acid oxidation disorders;Rinaldo;Annu. Rev. Physiol.,2002
2. A rare disease-associated mutation in the medium chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD);Andresen;Am. J. Hum. Genet.,1993
3. A silent A to G mutation in exon11 of the medium-chain acyl-CoA dehydrogenase (MCAD) gene;Andresen;Hum. Mol. Genet.,1993
4. Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old woman;Raymond;Genet. Med.,1999
5. Adult presentation of MCAD deficiency revealed by coma and severe arrythmias;Feillet;Intensive Care Med.,2003
Cited by
45 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