Mutation of a potassium channel-related gene in progressive myoclonic epilepsy-Reference-Cited by-同舟云学术

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Mutation of a potassium channel-related gene in progressive myoclonic epilepsy

Published:2007-04-23 Issue:6 Volume:61 Page:579-586
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Van Bogaert Patrick,Azizieh Regis,Désir Julie,Aeby Alec,De Meirleir Linda,Laes Jean-François,Christiaens Florence,Abramowicz Marc J.

Funder

Fonds pour la formation à la Recherche dans l'Industrie et dans l'Agriculture (FRIA)

Belgian Kids' Fund

Fonds de la Recherche Scientifique Médicale (FRSM)

Crédit Transdisciplinaire of the Fonds Erasme

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference31 articles.

1. Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children;Lander;Science,1987

2. Progressive myoclonus epilepsies: specific causes and diagnosis;Berkovic;N Engl J Med,1986

3. Progressive myoclonic epilepsy;Zupanc;Cerebellum,2004

4. Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects;Shahwan;Lancet Neurol,2005

5. Clinical presentations and phenomenology of myoclonus;Faught;Epilepsia,2003

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