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Results 1 - 10 of 10 for Spinocerebellar ataxia 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. ATXN2 gene 
    ... Gotay D, Jorge Cedeno H. Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in Holguin. Neurosci Lett. 2009 Apr 24;454(2):157-60. doi: 10.1016/j.neulet.2009.03.015. Epub 2009 Mar 11. Citation on PubMed
    https://medlineplus.gov/genetics/gene/atxn2 - Genetics
  4. Spinocerebellar ataxia type 2 
    ... Gotay D, Jorge Cedeno H. Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in Holguin. Neurosci Lett. 2009 Apr 24;454(2):157-60. doi: 10.1016/j.neulet.2009.03.015. Epub 2009 Mar 11. Citation on PubMed Velazquez-Perez L, Rodriguez-Labrada ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  5. 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
  6. Friedreich ataxia 
    ... and symptoms of the condition. FA FRDA Friedreich spinocerebellar ataxia Friedrich's ataxia ... A structural approach to understanding the iron-binding properties of phylogenetically different frataxins. Hum Mol Genet. 2002 Aug 1;11(16):1865-77. doi: 10.1093/hmg/11. ...
    https://medlineplus.gov/genetics/condition/friedreich-ataxia - Genetics
  7. 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 Genetic Testing Registry: ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  8. TWNK gene 
    ... gene have been found to cause infantile-onset spinocerebellar ataxia (IOSCA). The most common mutation replaces the protein ... Lonnqvist T, Spelbrink JN, Suomalainen A. Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with ...
    https://medlineplus.gov/genetics/gene/twnk - Genetics
  9. ATXN3 gene 
    ... regulating the first stage of protein production (transcription). Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by ... doi: 10.1093/hmg/ddi472. Epub 2006 Jan 11. Citation on PubMed Nicastro G, Masino L, Esposito ...
    https://medlineplus.gov/genetics/gene/atxn3 - Genetics
  10. CACNA1A gene 
    ... swelling and coma. More About This Health Condition Spinocerebellar ataxia type 6 (SCA6) is another disorder caused by ... epilepsy with infantile spasms. Epilepsia. 2009 Nov;50(11):2501-3. doi: 10.1111/j.1528-1167. ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics