Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 9 of 9 for Spinocerebellar ataxia type 11
  1. Spinocerebellar ataxia type 36 
    ... of the abnormal hexanucleotide GGCCUG repeat expansion in spinocerebellar ataxia type 36 (Asidan). Eur J Neurol. 2014 Nov;21(11):1377-86. doi: 10.1111/ene.12491. Epub ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  2. NOP56 gene 
    ... of the abnormal hexanucleotide GGCCUG repeat expansion in spinocerebellar ataxia type 36 (Asidan). Eur J Neurol. 2014 Nov;21(11):1377-86. doi: 10.1111/ene.12491. Epub ...
    https://medlineplus.gov/genetics/gene/nop56 - Genetics
  3. Spinocerebellar ataxia type 2 
    Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition initially ... s mother (maternal inheritance). SCA2 Genetic Testing Registry: Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 2 National Organization for ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  4. TPP1 gene 
    ... de Warrenburg BP, Maat-Kievit AJ. Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is ... 2013 Mar 11. Citation on PubMed
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  5. Ataxia with oculomotor apraxia 
    ... with ocular motor apraxia and hypoalbuminemia SCAN2 SCAR1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia, recessive, non-Friedreich type 1 ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  6. ATXN2 gene 
    ... is repeated approximately 22 times within the gene. Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive ... Gotay D, Jorge Cedeno H. Molecular epidemiology of spinocerebellar ataxias in Cuba: ... Epub 2009 Mar 11. Citation on PubMed
    https://medlineplus.gov/genetics/gene/atxn2 - Genetics
  7. ATXN3 gene 
    ... regulating the first stage of protein production (transcription). Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by progressive ...
    https://medlineplus.gov/genetics/gene/atxn3 - Genetics
  8. CACNA1A gene 
    ... swelling and coma. More About This Health Condition Spinocerebellar ataxia type 6 (SCA6) is another disorder caused by CACNA1A ... 21. doi: 10.1038/nature12439. Epub 2013 Aug 11. Citation on PubMed or Free ... episodic ataxia type 2 mutations involve disruption of membrane trafficking of ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  9. TWNK gene 
    ... gene have been found to cause infantile-onset spinocerebellar ataxia (IOSCA). The most common mutation replaces the protein ... 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