SCN4Apore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy-Reference-Cited by-同舟云学术

SCN4Apore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy

Published:2015-10-01 Issue: Volume: Page:ddv410
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Bergareche Alberto,Bednarz Marcin,Sánchez Elena,Krebs Catharine E.,Ruiz-Martinez Javier,De La Riva Patricia,Makarov Vladimir,Gorostidi Ana,Jurkat-Rott Karin,Marti-Masso Jose Felix,Paisán-Ruiz Coro

Funder

Instituto de Salud Carlos III

non-profit Hertie foundation

IonNeurONet

German Federal Research Ministry of Research

National Institute of Neurological Disorders and Stroke

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/24/24/7111/17263016/ddv410.pdf

Reference56 articles.

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4. Essential tremor: a neurodegenerative disease?;Benito-Leon;Tremor Other Hyperkinet. Mov.,2014

5. Genetics of essential tremor: Meta-analysis and review

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