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1 Possible Causes for Caused by Mutation in the CWF19-Like Protein 1 Gene, Cerebellar Hypoplasia Predominantly Affecting the Vermis

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    Alendar A, Euljkovic B, Savic D, Djarmati A, Keckarevic M, Ristic A, Dragasevic N, Kosic V, Romac S. Spinocerebellar ataxia type 17 in the Yugoslav population. Acta Neurol Scand. 2004; 109 :185–7. [ PubMed : 14763955 ] Bauer P, Laccone F, Rolfs A, Wullner U, Bosch S, Peters H, Liebscher S, Scheible M, Epplen JT, Weber BH,[…][ncbi.nlm.nih.gov]

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