An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains
- 1 August 2005
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 77 (2), 280-296
- https://doi.org/10.1086/432518
Abstract
No abstract availableKeywords
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