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Results 1 - 2 of 2 for Autosomal recessive spinocerebellar ataxia 13
  1. TPP1 gene 
    ... JT, van de Warrenburg BP, Maat-Kievit AJ. Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease). Hum Mutat. 2013 May;34(5):706-13. doi: 10.1002/humu.22292. Epub 2013 Mar ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  2. Autosomal recessive cerebellar ataxia type 1 
    ... show signs and symptoms of the condition. ARCA1 Autosomal recessive spinocerebellar ataxia 8 Recessive ataxia of Beauce Genetic Testing Registry: ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8 PubMed Beaudin M, Gamache PL, Gros- ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics