Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
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| Description | scientific article published on 7 April 2016 |
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author: Raffaella Cusmai Sabina Barresi Marcello Niceta Alessandro Bruselles Marco Tartaglia Ginevra Zanni Enrico Bertini |
| Publication date | May 11, 2016 |
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