Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
Open Access
- 1 November 2014
- journal article
- case report
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 95 (5), 611-621
- https://doi.org/10.1016/j.ajhg.2014.10.007
Abstract
No abstract availableKeywords
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