A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference19 articles.
1. Benign familial neonatal convulsions linked to genetic markers on chromosome 20;Leppert;Nature,1989
2. Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity;Ryan;Ann. Neurol.,1991
3. Classification of familial neonatal convulsions;Wakai;Lancet,1994
4. Seizure characteristics in chromosome 20 benign familial neonatal convulsions;Ronen;Neurology,1993
5. Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q;Lewis;Am. J. Hum. Genet.,1993
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