Spinocerebellar Ataxia type 29 in a family of Māori descent

Spinocerebellar Ataxia type 29 in a family of Māori descent

Abstract Background Mutations in the Inositol 1,4,5-Trisphosphate Receptor Type 1 (ITPR1) gene cause spinocerebellar ataxia type 29 (SCA29), a rare congenital-onset autosomal dominant non-progressive cerebellar ataxia. The Māori, indigenous to New Zealand, are an understudied population for genetic...

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Bibliographic Details
Main Authors: Kathie J. Ngo, Gemma Poke, Katherine Neas, Brent L. Fogel
Format: Article
Language:English
Published: BMC 2019-10-01
Series:Cerebellum & Ataxias
Subjects:
Cerebellar Ataxia
Spinocerebellar Ataxia
SCA29
Neurogenetics
Gait disorders/ataxia
Māori
Online Access:http://link.springer.com/article/10.1186/s40673-019-0108-3

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http://link.springer.com/article/10.1186/s40673-019-0108-3

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