Inherited disorders of gamma-aminobutyric acid metabolism and advances inALDH5A1mutation identification-Reference-Cited by-同舟云学术

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Inherited disorders of gamma-aminobutyric acid metabolism and advances inALDH5A1mutation identification

Published:2014-12-29 Issue:7 Volume:57 Page:611-617
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Dev Med Child Neurol

Author:

Pearl Phillip L¹,Parviz Mahsa¹,Vogel Kara²,Schreiber John³,Theodore William H⁴,Gibson K Michael²

Affiliation:

1. Department of Neurology; Boston Children's Hospital; Harvard Medical School; Boston MA USA

2. Department of Experimental and Systems Pharmacology; College of Pharmacy; Washington State University; Spokane WA USA

3. Department of Neurology; Children's National Medical Center; Washington DC USA

4. Clinical Epilepsy Branch; NINDS; NIH; Bethesda MD USA

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/dmcn.12668/fullpdf

Reference61 articles.

1. gamma-Aminobutyric acid in brain: its formation from glutamic acid;Roberts;J Biol Chem,1950

2. The excitation and depression of spinal neurones by structurally related amino acids;Curtis;J Neurochem,1960

3. The action of gamma-aminobutyric acid on cortical neurones;Krnjevic;Exp Brain Res,1967

4. Defects in GABA metabolism affect selective autophagy pathways and are alleviated by mTOR inhibition;Lakhani;EMBO Mol Med,2014

5. GAT-1, a high-affinity GABA plasma membrane transporter, is localized to neurons and astroglia in the cerebral cortex;Minelli;J Neurosci,1995

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