A Novel Splicing Mutation in KCNQ2 in a Multigenerational Family with BFNC Followed for 25 Years-Reference-Cited by-同舟云学术

A Novel Splicing Mutation in KCNQ2 in a Multigenerational Family with BFNC Followed for 25 Years

Published:2006-05 Issue:5 Volume:47 Page:851-859
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

de Haan Gerrit-Jan,Pinto Dalila,Carton Dietbrandt,Bader Adri,Witte Jorien,Peters Edith,van Erp Gerard,Vandereyken Willem,Boezeman Eduard,Wapenaar Martin C.,Boon Paul,Halley Dicky,Koeleman Bobby P. C.,Lindhout Dick

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2006.00552.x/fullpdf

Reference50 articles.

1. Benign Familial Neonatal Convulsions

2. Benign familial neonatal convulsions linked to genetic markers on chromosome 20

3. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

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3. Genetics of Photosensitivity;The Importance of Photosensitivity for Epilepsy;2020-12-24

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