1-1 of 1
Keywords: DYT1
Follow your search
Access your saved searches in your account

Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Biochem Soc Trans (2010) 38 (2): 452–456.
Published: 22 March 2010
...Thomas T. Warner; Alassandra Granata; Giampietro Schiavo DYT1 dystonia is an autosomal dominant movement disorder, characterized by early onset of involuntary sustained muscle contractions. It is caused by a 3-bp deletion in the DYT1 gene, which results in the deletion of a single glutamate residue...