Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene-Reference-Cited by-同舟云学术

Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene

Published:2017-02 Issue:2 Volume:39 Page:161-165
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Nagappa Madhu,Bindu Parayil Sankaran,Chiplunkar Shwetha,Govindaraj Periasamy,Narayanappa Gayathri,Krishnan Ayyappan,Bharath M.M. Srinivas,Swaminathan Aarthi,Saini Jitender,Arvinda Hanumanthapura R.,Sinha Sanjib,Mathuranath Pavagada S.,Taly Arun B.

Funder

Indian Council for Medical Research

Government of India

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

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3. A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy;Tsuji;J Inherit Metab Dis,2010

4. The GABA transaminase, ABAT, is essential for mitochondrial nucleoside metabolism;Besse;Cell Metab,2015

5. Role of GABAA receptors in the physiology and pharmacology of sleep;Winsky-Sommerer;Eur J Neurosci,2009

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