TY - JOUR AU - Ngo, Kathie J. AU - Poke, Gemma AU - Neas, Katherine AU - Fogel, Brent L. PY - 2019 DA - 2019/10/12 TI - Spinocerebellar Ataxia type 29 in a family of Māori descent JO - Cerebellum & Ataxias SP - 14 VL - 6 IS - 1 AB - 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 ataxias. SN - 2053-8871 UR - https://doi.org/10.1186/s40673-019-0108-3 DO - 10.1186/s40673-019-0108-3 ID - Ngo2019 ER -