DOI:
10.1055/s-00029025
Journal of Pediatric Epilepsy
LinksClose Window
References
Nagappa M, Bindu PS, Chiplunkar S. et al.
Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene.
Brain Dev 2017;
39 (02) 161-165
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.