De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene
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A. Munnich | N. Boddaert | S. Hanein | M. Shinawi | P. Lory | C. Bole-Feysot | P. Nitschké | J. Thevenon | S. Lyonnet | L. Faivre | H. Zimmerman | I. Desguerre | L. Colleaux | E. Fassi | P. Blanc | N. Bahi-Buisson | J. Amiel | M. Rio | G. Barcia | J. Chemin | L. Hubert | V. Cantagrel | K. Siquier-Pernet | Daniel Medina-Cano | M. Nicouleau | Céline Vidal | A. Ahmad | Nami Altin | Cécile Fourage | Vincent Cantagrel | C. Bôle-Feysot
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