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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
Author/s
author: Daniel Medina-Cano, Pierre Blanc, Philippe Lory, Vincent Cantagrel, Sylvain Hanein, Arnold Munnich
Work details
Publication date
July 1, 2018
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Language
English
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