A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia-Reference-Cited by-同舟云学术

A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia

Published:2015-11 Issue:5 Volume:97 Page:726-737
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Coutelier Marie,Blesneac Iulia,Monteil Arnaud,Monin Marie-Lorraine,Ando Kunie,Mundwiller Emeline,Brusco Alfredo,Le Ber Isabelle,Anheim Mathieu,Castrioto Anna,Duyckaerts Charles,Brice Alexis,Durr Alexandra,Lory Philippe,Stevanin Giovanni

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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