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eNauka >  Results >  Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia
Title: Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia
Authors: Barresi, S; Niceta, M; Alfieri, P; Brankovic, Vesna; Piccini, G; Bruselles, A; Barone, MR; Cusmai, Raffaella; Tartaglia, M; Bertini, E;
Zanni, G;
Issue Date: 2017
Publication: CLINICAL GENETICS
ISSN: 0009-9163 Clinical Genetics Search Idenfier
Type: Article
Collation: vol. 91 br. 1 str. 86-91
DOI: 10.1111/cge.12783
WoS-ID: 000393979600011
Scopus-ID: 2-s2.0-84966573792
URI: https://enauka.gov.rs/handle/123456789/830298
Project: Italian Telethon Foundation [GGP08145]
Metadata source: (Preuzeto iz Nasi u WoS)
M-category: 
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