A primigravida with very-long-chain acyl-CoA dehydrogenase deficiency-Reference-Cited by-同舟云学术

A primigravida with very-long-chain acyl-CoA dehydrogenase deficiency

Published:2014-01-16 Issue:2 Volume:49 Page:295-296
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Murata Ken-ya¹,Sugie Hideo²,Nishino Ichizo³,Kondo Tomoyoshi¹,Ito Hidefumi¹

Affiliation:

1. Department of Neurology; Wakayama Medical University; Wakayama Japan

2. Department of Pediatrics; Jichi Medical University; Tochigi Japan

3. Department of Neuromuscular Research, National Institute of Neuroscience; National Center for Neurology and Psychiatry; Tokyo Japan

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.24055/fullpdf

Reference13 articles.

1. Clinical and molecular heterogeneity in very-long-chain acyl-coenzyme A dehydrogenase deficiency;Pons;Pediatr Neurol,2000

2. Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase;Izai;J Biol Chem,1992

3. Assay of acyl-CoA dehydrogenase activity in frozen muscle biopsies: application to medium-chain acyl-CoA dehydrogenase deficiency;Verity;Biochem Med Metab Biol,1993

4. Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene;Andresen;Hum Mol Genet,1996

5. Genomic DNA organization of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis;Orii;Biochem Biophys Res Commun,1995

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