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Expanded molecular features of carnitine acyl-carnitine translocase (CACT) deficiency by comprehensive molecular analysis

  • Published:2011-08 Issue:4 Volume:103 Page:349-357
  • ISSN:1096-7192
  • Container-title:Molecular Genetics and Metabolism
  • language:en
  • Short-container-title:Molecular Genetics and Metabolism

Author:

Wang Guo-li,Wang Jing,Douglas Ganka,Browning Marsha,Hahn Sihoun,Ganesh Jaya,Cox Sarah,Aleck Kirk,Schmitt Eric S.,Zhang Wei,Wong Lee-Jun C.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference26 articles.

1. Mitochondrial fatty acid oxidation disorders;Chace,2001

2. Kinetic compartmental analysis of carnitine metabolism in the human carnitine deficiency syndromes. Evidence for alterations in tissue carnitine transport.;Rebouche;J. Clin. Invest.,1984

3. Carnitine deficiency disorders in children;Stanley;Ann. N.Y. Acad. Sci.,2004

4. Carnitine in neonatal nutrition;Borum;J. Child Neurol.,1995

5. Primary and secondary alterations of neonatal carnitine metabolism;Scaglia;Semin. Perinatol.,1999
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