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Are (CTG)n expansions at the SCA8 locus rare polymorphisms?
Stevanin G, Herman A, Dürr A, Jodice C, Frontali M, Agid Y, Brice A. Stevanin G, et al. Among authors: brice a. Nat Genet. 2000 Mar;24(3):213; author reply 215. doi: 10.1038/73408. Nat Genet. 2000. PMID: 10700167 No abstract available.
More missense in amyloid gene.
Carter DA, Desmarais E, Bellis M, Campion D, Clerget-Darpoux F, Brice A, Agid Y, Jaillard-Serradt A, Mallet J. Carter DA, et al. Among authors: brice a. Nat Genet. 1992 Dec;2(4):255-6. doi: 10.1038/ng1292-255. Nat Genet. 1992. PMID: 1303275 No abstract available.
Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutation.
Stevanin G, Cancel G, Didierjean O, Dürr A, Abbas N, Cassa E, Feingold J, Agid Y, Brice A. Stevanin G, et al. Among authors: brice a. Am J Hum Genet. 1995 Nov;57(5):1247-50. Am J Hum Genet. 1995. PMID: 7485178 Free PMC article. No abstract available.
Gender equality in Machado-Joseph disease.
Dürr A, Stevanin G, Cancel G, Abbas N, Chneiweiss H, Agid Y, Feingold J, Brice A. Dürr A, et al. Among authors: brice a. Nat Genet. 1995 Oct;11(2):118-9. doi: 10.1038/ng1095-118a. Nat Genet. 1995. PMID: 7550335 No abstract available.
Diagnosis of "sporadic" Huntington's disease.
Dürr A, Dodé C, Hahn V, Pêcheux C, Pillon B, Feingold J, Kaplan JC, Agid Y, Brice A. Dürr A, et al. Among authors: brice a. J Neurol Sci. 1995 Mar;129(1):51-5. doi: 10.1016/0022-510x(94)00250-r. J Neurol Sci. 1995. PMID: 7751845
1,073 results