De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene (Q89022033)
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scientific article published on 01 July 2018
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene |
scientific article published on 01 July 2018 |
Statements
De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene (English)
Sylvain Hanein
Jean Chemin
Karine Siquier-Pernet
Michaël Nicouleau
Giulia Barcia
Ali Ahmad
Nami Altin
Laurence Hubert
Christine Bole-Feysot
Cécile Fourage
Patrick Nitschké
Julien Thevenon
Marlène Rio
Céline Vidal
Nadia Bahi-Buisson
Isabelle Desguerre
Stanislas Lyonnet
Nathalie Boddaert
Emily Fassi
Marwan Shinawi
Holly Zimmerman
Jeanne Amiel
Laurence Faivre
Laurence Colleaux