A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice-Reference-Cited by-同舟云学术

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A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice

Published:2010-12-15 Issue:5 Volume:20 Page:988-999
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Tokuda S.,Mahaffey C. L.,Monks B.,Faulkner C. R.,Birnbaum M. J.,Danzer S. C.,Frankel W. N.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/20/5/988/7071586/ddq544.pdf

Reference41 articles.

1. Impact of our understanding of the genetic aetiology of epilepsy

2. Genetic Polymorphisms and Idiopathic Generalized Epilepsies

3. Three ENU-induced neurological mutations in the pore loopof sodium channel Scn8a (Na v 1.6) and a genetically linkedretinal mutation, rd13

4. Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

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