De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene
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| Description | scientific article published on 01 July 2018 |
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author: Daniel Medina-Cano Pierre Blanc Vincent Cantagrel Philippe Lory Arnold Munnich Sylvain Hanein |
| Publication date | July 1, 2018 |
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