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Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene |
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Titel: |
Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene |
Auteur: |
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. |
Verschenen in: |
Brain & development |
Paginering: |
Jaargang 39 (2017) nr. 2 pagina's 5 p. |
Jaar: |
2017 |
Inhoud: |
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Uitgever: |
The Japanese Society of Child Neurology |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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