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Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred.
Kwiatkowski DJ, Nygaard TG, Schuback DE, Perman S, Trugman JM, Bressman SB, Burke RE, Brin MF, Ozelius L, Breakefield XO, et al. Kwiatkowski DJ, et al. Among authors: bressman sb. Am J Hum Genet. 1991 Jan;48(1):121-8. Am J Hum Genet. 1991. PMID: 1985454 Free PMC article.
Human gene for torsion dystonia located on chromosome 9q32-q34.
Ozelius L, Kramer PL, Moskowitz CB, Kwiatkowski DJ, Brin MF, Bressman SB, Schuback DE, Falk CT, Risch N, de Leon D, et al. Ozelius L, et al. Among authors: bressman sb. Neuron. 1989 May;2(5):1427-34. doi: 10.1016/0896-6273(89)90188-8. Neuron. 1989. PMID: 2576373
Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms.
Breakefield XO, Bressman SB, Kramer PL, Ozelius L, Moskowitz C, Tanzi R, Brin MF, Hobbs W, Kaufman D, Tobin A, et al. Breakefield XO, et al. Among authors: bressman sb. J Neurogenet. 1986 May;3(3):159-75. doi: 10.3109/01677068609106846. J Neurogenet. 1986. PMID: 3016220
Paroxysmal non-kinesigenic dystonia.
Bressman SB, Fahn S, Burke RE. Bressman SB, et al. Adv Neurol. 1988;50:403-13. Adv Neurol. 1988. PMID: 3400499
164 results