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Spinocerebellar ataxia 19
- ... 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 ...
- ... 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- ...
- ... with hypogonadism and choroidal dystrophy syndrome Chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism Spinocerebellar ataxia, hypogonadotropic hypogonadism, and ...
- ... 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 ...
- ... 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. ...