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Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene by 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. is a Medicine article available to read on EtoBox.

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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.
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 0387-7604)
Published
2016
Language
EN
Field
Medicine (Health Sciences)

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