Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females-Reference-Cited by-同舟云学术

Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females

Published:2010-11-04 Issue:1 Volume:32 Page:E1959-E1975
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Depienne Christel,Trouillard Oriane,Bouteiller Delphine,Gourfinkel-An Isabelle,Poirier Karine,Rivier François,Berquin Patrick,Nabbout Rima,Chaigne Denys,Steschenko Dominique,Gautier Agnès,Hoffman-Zacharska Dorota,Lannuzel Annie,Lackmy-Port-Lis Marilyn,Maurey Hélène,Dusser Anne,Bru Marie,Gilbert-Dussardier Brigitte,Roubertie Agathe,Kaminska Anna,Whalen Sandra,Mignot Cyril,Baulac Stéphanie,Lesca Gaetan,Arzimanoglou Alexis,LeGuern Eric

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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