DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
LinksClose Window
References
Meng H, Xu HQ, Yu L. et al.
The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype.
Hum Mutat 2015;
36 (06) 573-580
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.