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 - 10 of 10 for Spinocerebellar ataxia type 12
  1. Spinocerebellar ataxia type 2 
    ... j.jns.2009.12.013. Epub 2010 Jan 12. Citation on PubMed
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  2. Spinocerebellar ataxia type 1 
    ... Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1. J Biol Chem. 2009 Mar 20;284(12):7425-9. doi: 10.1074/jbc.R800041200. Epub ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  3. ATXN1 gene 
    ... Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1. J Biol Chem. 2009 Mar 20;284(12):7425-9. doi: 10.1074/jbc.R800041200. Epub ...
    https://medlineplus.gov/genetics/gene/atxn1 - Genetics
  4. Spinocerebellar ataxia type 3 
    Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  5. TPP1 gene 
    ... AM, Noher de Halac I. Neuronal ceroid lipofuscinosis type CLN2: a new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America. Gene. 2013 Mar 1;516(1):114-21. doi: 10.1016/j.gene.2012.12.058. Epub 2012 Dec 22. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  6. 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
  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 ... novo mutations in epileptic encephalopathies. Nature. 2013 Sep ... episodic ataxia type 2 mutations involve disruption of membrane trafficking of ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  9. ABCB7 gene 
    ... a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia. J Hum Genet. ... 2002 Dec 12. Citation on PubMed
    https://medlineplus.gov/genetics/gene/abcb7 - Genetics
  10. Primary coenzyme Q10 deficiency 
    ... 78-87. doi: 10.1016/j.biochi.2013.12.006. Epub 2013 Dec 16. Citation on PubMed ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics