Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures-Reference-Cited by-同舟云学术

Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures

Published:2010-08-02 Issue:2 Volume:80 Page:191-195
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Bartnik M,Chun-Hui Tsai A,Xia Z,Cheung SW,Stankiewicz P

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01526.x/fullpdf

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4. Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy.;Holland;Neurosci Lett,2008

5. The spectrum of SCN1A-related infantile epileptic encephalopathies.;Harkin;Brain,2007

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