Sadewa AH et al. (2008). Germ-line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion. Pediatrics international : official journal of the Japan Pediatric Society. 50 [PubMed]

See more from authors: Sadewa AH · Sasongko TH · Gunadi · Lee MJ · Daikoku K · Yamamoto A · Yamasaki T · Tanaka S · Matsuo M · Nishio H

References and models cited by this paper
References and models that cite this paper

Miceli F et al. (2013). Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits. Proceedings of the National Academy of Sciences of the United States of America. 110 [PubMed]

Miceli F et al. (2009). Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures. Neurobiology of disease. 34 [PubMed]

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