Hyperglycosylation and Reduced GABA Currents of Mutated GABRB3 Polypeptide in Remitting Childhood Absence Epilepsy-Reference-Cited by-同舟云学术

Hyperglycosylation and Reduced GABA Currents of Mutated GABRB3 Polypeptide in Remitting Childhood Absence Epilepsy

Published:2008-06 Issue:6 Volume:82 Page:1249-1261
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Tanaka Miyabi,Olsen Richard W.,Medina Marco T.,Schwartz Emily,Alonso Maria Elisa,Duron Reyna M.,Castro-Ortega Ramon,Martinez-Juarez Iris E.,Pascual-Castroviejo Ignacio,Machado-Salas Jesus,Silva Rene,Bailey Julia N.,Bai Dongsheng,Ochoa Adriana,Jara-Prado Aurelio,Pineda Gregorio,Macdonald Robert L.,Delgado-Escueta Antonio V.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference60 articles.

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3. Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies;Haug;Nat. Genet.,2003

4. A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy;Maljevic;Ann. Neurol.,2006

5. Familial occurrence of epilepsy in children with newly diagnosed multiple seizures: Dutch Study of Epilepsy in Childhood;Callenbach;Epilepsia,1998

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