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 - 5 of 5 for Spinocerebellar ataxia 19
  1. Infantile-onset spinocerebellar ataxia 
    ... 20. Citation on PubMed Lonnqvist T. Infantile-Onset Spinocerebellar Ataxia. 2009 Jan 27 [updated 2018 Apr 19]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  2. Spinocerebellar ataxia type 36 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov ... and affective impairments of a novel SCA/MND crossroad mutation Asidan. Eur J Neurol. 2012 Aug;19(8):1070-8. doi: 10.1111/j.1468- ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  3. Boucher-Neuhäuser syndrome 
    ... with hypogonadism and choroidal dystrophy syndrome Chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism Spinocerebellar ataxia, hypogonadotropic hypogonadism, and ...
    https://medlineplus.gov/.../condition/boucher-neuhauser-syndrome - Genetics
  4. TPP1 gene 
    ... TPP1 gene have also been found to cause spinocerebellar ataxia, autosomal recessive 7 (SCAR7), which is a condition ... Tests of TPP1 PubMed TRIPEPTIDYL PEPTIDASE I; TPP1 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7 NCBI Gene ClinVar Elleder ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  5. CACNA1A gene 
    ... swelling and coma. More About This Health Condition Spinocerebellar ataxia type 6 (SCA6) is another disorder caused by ... gene is located in a region of chromosome 19 that is missing in most people with 19p13. ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics