Autori: Tartaglia M
| Naslov | Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia (Article) |
| Autori | Barresi S Niceta M Alfieri P Brankovic Vesna Piccini G Bruselles A Barone MR Cusmai Raffaella Tartaglia M Bertini E Zanni G |
| Info | CLINICAL GENETICS, (2017), vol. 91 br. 1, str. 86-91 |
| Projekat | Italian Telethon Foundation [GGP08145] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
