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Spinocerebellar Ataxia type 29 in a family of Māori descent
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 ataxias....
Gorde:
| Argitaratua izan da: | Cerebellum Ataxias |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2019
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6790028/ https://ncbi.nlm.nih.gov/pubmed/31632679 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40673-019-0108-3 |
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