Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia-Reference-Cited by-同舟云学术

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

Published:2017-05 Issue:3 Volume:21 Page:450-456
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Travaglini Lorena,Nardella Marta,Bellacchio Emanuele,D'Amico Adele,Capuano Alessandro,Frusciante Roberto,Di Capua Matteo,Cusmai Raffaella,Barresi Sabina,Morlino Silvia,Fernández-Fernández José M.,Trivisano Marina,Specchio Nicola,Valeriani Massimiliano,Vigevano Federico,Bertini Enrico,Zanni Ginevra

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

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