Missense mutations of CACNA1A are a frequent cause of...

European Journal of Paediatric Neurology 2017 / 05 Vol. 21; Iss. 3

Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Travaglini, Lorena, Nardella, Marta, Bellacchio, Emanuele, D'Amico, Adele, Capuano, Alessandro, Frusciante, Roberto, Di Capua, Matteo, Cusmai, Raffaella, Barresi, Sabina, Morlino, Silvia, Fernández-Fe
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Volume:
21
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/j.ejpn.2016.11.005
Date:
May, 2017
File:
PDF, 1.37 MB
english, 2017
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