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Results 1 - 5 of 5 for Spinocerebellar ataxia type 29
  1. ITPR1 gene 
    ... in people with spinocerebellar ataxia type 15 (SCA15), spinocerebellar ataxia type 29 (SCA29), and less commonly, in other forms of ... spinocerebellar ataxias. IP3R IP3R1 Tests of ... SPINOCEREBELLAR ATAXIA 29; SCA29 INOSITOL 1,4,5-TRIPHOSPHATE RECEPTOR, TYPE 1; ITPR1 SPINOCEREBELLAR ATAXIA 15; SCA15 NCBI Gene ...
    https://medlineplus.gov/genetics/gene/itpr1 - Genetics
  2. Huntington's disease-like 
    ... Onodera O, Yamada M, Tsuji S, Takahashi H. Spinocerebellar Ataxia Type 17. 2005 Mar 29 [updated 2022 Jul 28]. In: Adam MP, Feldman ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease-like - Genetics
  3. CACNA1A gene 
    ... swelling and coma. More About This Health Condition Spinocerebellar ataxia type 6 (SCA6) is another disorder caused by CACNA1A ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  4. TWNK gene 
    ... doi: 10.1212/WNL.0000000000001036. Epub 2014 Oct 29. Citation on PubMed or Free article on PubMed Central Nikali K, Suomalainen A, Saharinen J, Kuokkanen M, Spelbrink JN, Lonnqvist T, Peltonen L. Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins ...
    https://medlineplus.gov/genetics/gene/twnk - Genetics
  5. Primary coenzyme Q10 deficiency 
    ... deficiencies and related nephropathies. Pediatr Nephrol. 2014 Jun;29(6):961-9. doi: 10.1007/s00467-013- ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics