Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation-Reference-Cited by-同舟云学术

Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation

Published:2014-02-05 Issue:13 Volume:23 Page:3481-3489
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Lee Hane,Lin Meng-chin A.,Kornblum Harley I.,Papazian Diane M.,Nelson Stanley F.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/23/13/3481/19637852/ddu056.pdf

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4. Observation of a New chi_{b} State in Radiative Transitions to Upsilon(1S) and Upsilon(2S) at ATLAS;Aad;Phys. Rev. Lett.,2012

5. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations;O'Roak;Nat. Genet.,2011

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