학술논문
Cryptic chromosome deletions involving SCN1Ain severe myoclonic epilepsy of infancy
Document Type
Article
Author
Source
Neurology (Ovid); October 2006, Vol. 67 Issue: 7 p1230-1235, 6p
Subject
Language
ISSN
00283878; 1526632X
Abstract
To identify cryptic chromosomal deletions involving SCN1Ain patients with severe myoclonic epilepsy of infancy (SMEI).