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  1. A number sign (#) is used with this entry because of evidence that torsion dystonia-1 (DYT1) is caused by heterozygous mutation in the TOR1A gene (605204), encoding the ATP-binding protein torsin-A, on chromosome 9q34. 14: 177-187, 1976.[Pub Med: 941771]" pmid="941771"Nemeth, 2002). In a large North American family of non-Jewish ancestry, Autosomal dominant dystonia in a large North American family: clinical features. In 23 of the 70 noncarriers, the disease was familial and included brachial, cervical, laryngeal, and facial dystonia. (1996) studied 49 probands with cervical or cranial dystonia with age of onset greater than 12 years and with a positive family history.