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Results 1 - 4 of 4 for Spinocerebellar ataxia type 36
  1. Spinocerebellar ataxia type 36 
    Spinocerebellar ataxia type 36 (SCA36) is a condition characterized by progressive problems with movement that typically begin in mid-adulthood. People with this condition ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  2. NOP56 gene 
    ... repeated hexanucleotide is unclear. NOP56 gene mutations cause spinocerebellar ataxia type 36 (SCA36), which is a condition characterized by progressive ...
    https://medlineplus.gov/genetics/gene/nop56 - Genetics
  3. Movement Disorders (National Library of Medicine)  
    Movement disorders are neurologic conditions that cause problems with movement, such as: Increased movement that can be voluntary (intentional) or involuntary ( ...
    https://medlineplus.gov/movementdisorders.html - Health Topics
  4. Infantile-onset spinocerebellar ataxia 
    ... Testing Registry: Infantile onset spinocerebellar ataxia Infantile-onset ... with autosomal, X-chromosomal or maternal inheritance. Can J Neurol Sci. 2009 Jul;36(4):409-28. doi: 10.1017/s0317167100007733. Citation ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics