DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
Vetri L, Calì F, Vinci M. et al.
A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy.
Eur J Med Genet 2020;
63 (04) 103848
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.