학술논문
Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures.
Document Type
Article
Author
Source
Molecular Syndromology; Sep2016, Vol. 7 Issue 4, p189-196, 8p
Subject
Language
ISSN
16618769