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Familial non-specific dementia maps to chromosome 3.
Brown J, Ashworth A, Gydesen S, Sorensen A, Rossor M, Hardy J, Collinge J. Brown J, et al. Hum Mol Genet. 1995 Sep;4(9):1625-8. doi: 10.1093/hmg/4.9.1625. Hum Mol Genet. 1995. PMID: 8541850
Genetic characterization of a novel familial dementia.
Brown J, Smith S, Brun A, Collinge J, Gydesen S, Hardy J, Mullan M, Goate A. Brown J, et al. Ann N Y Acad Sci. 1991;640:181-3. doi: 10.1111/j.1749-6632.1991.tb00213.x. Ann N Y Acad Sci. 1991. PMID: 1776737
G/T polymorphism in CRYA2 gene.
Ashworth A, Campbell T, Palmer M, Collinge J, Brown J. Ashworth A, et al. Among authors: brown j. Hum Mol Genet. 1994 Sep;3(9):1712. doi: 10.1093/hmg/3.9.1712. Hum Mol Genet. 1994. PMID: 7833944 No abstract available.
Exclusion mapping in familial non-specific dementia.
Brown J, Gydesen S, Sorensen SA, Brun A, Duff K, Houlden H, Fidani L, Kullkarni S, Cummings J, Goate A, et al. Brown J, et al. Dementia. 1993 May-Aug;4(3-4):163-6. doi: 10.1159/000107317. Dementia. 1993. PMID: 8401786
Molecular genetic characterisation of frontotemporal dementia on chromosome 3.
Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V Jr, Taylor K, Cameron J, Munroe D, Johansson J, Rossor M, Fisher EM, Collinge J. Ashworth A, et al. Among authors: brown j. Dement Geriatr Cogn Disord. 1999;10 Suppl 1:93-101. doi: 10.1159/000051222. Dement Geriatr Cogn Disord. 1999. PMID: 10436350
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