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Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene
Nagappa, Madhu, Bindu, Parayil Sankaran, Chiplunkar, Shwetha, Govindaraj, Periasamy, Narayanappa, Gayathri, Krishnan, Ayyappan, Bharath, M.M. Srinivas, Swaminathan, Aarthi, Saini, Jitender, Arvinda, HLanguage:
english
Journal:
Brain and Development
DOI:
10.1016/j.braindev.2016.08.005
Date:
September, 2016
File:
PDF, 952 KB
english, 2016