@ARTICLE{
author={Barresi S,Niceta M,Alfieri P,Brankovic Vesna,Piccini G,Bruselles A,Barone MR,Cusmai Raffaella,Tartaglia M,Bertini E,Zanni G},
year={2017},
title={Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia},
journal={CLINICAL GENETICS},
volume={91},
number={1},
pages={86-91},
document_type={Article},
}