-
1
-
-
0027342814
-
Clinical features and classification of inherited ataxias
-
Harding AE. Clinical features and classification of inherited ataxias. Adv Neurol 1993;61:1-14.
-
(1993)
Adv Neurol
, vol.61
, pp. 1-14
-
-
Harding, A.E.1
-
2
-
-
0031710988
-
Unstable mutations and neurodegenerative disorders
-
Brice A. Unstable mutations and neurodegenerative disorders. J Neurol 1998;245:505-510.
-
(1998)
J Neurol
, vol.245
, pp. 505-510
-
-
Brice, A.1
-
3
-
-
0033069723
-
Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22
-
Zu L, Figueroa KP, Grewal R, Pulst SM. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22. Am J Hum Genet 1999;64:594-599.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 594-599
-
-
Zu, L.1
Figueroa, K.P.2
Grewal, R.3
Pulst, S.M.4
-
4
-
-
0028020605
-
Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
-
Ranum LP, Schut LJ, Lundgren JK, Orr HT, Livingston DM. Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11. Nat Genet 1994;8:280-284.
-
(1994)
Nat Genet
, vol.8
, pp. 280-284
-
-
Ranum, L.P.1
Schut, L.J.2
Lundgren, J.K.3
Orr, H.T.4
Livingston, D.M.5
-
5
-
-
0345199753
-
High-resolution genetic and physical mapping of spinocerebellar ataxia type 5 (SCA5) on 11q13
-
Abstract
-
Koob MD, Lundgren JK, Nowak NJ, et al. High-resolution genetic and physical mapping of spinocerebellar ataxia type 5 (SCA5) on 11q13. Am J Hum Genet 1995;57(suppl):A196. Abstract.
-
(1995)
Am J Hum Genet
, vol.57
, Issue.SUPPL.
-
-
Koob, M.D.1
Lundgren, J.K.2
Nowak, N.J.3
-
6
-
-
15844383259
-
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p1:3-11.q13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene
-
Pang JT, Lloyd SE, Wooding C, et al. Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p1:3-11.q13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene. Hum Genet 1996;97:732-741.
-
(1996)
Hum Genet
, vol.97
, pp. 732-741
-
-
Pang, J.T.1
Lloyd, S.E.2
Wooding, C.3
-
8
-
-
0343416801
-
Clinical and molecular features of spinocerebellar ataxia type 6
-
Stevanin G, Durr A, David G, et al. Clinical and molecular features of spinocerebellar ataxia type 6. Neurology 1997;49: 1243-1246.
-
(1997)
Neurology
, vol.49
, pp. 1243-1246
-
-
Stevanin, G.1
Durr, A.2
David, G.3
-
9
-
-
10544253082
-
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias
-
Stevanin G, Trottier Y, Cancel G, et al. Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias. Hum Mol Genet 1996;5:1887-1892.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1887-1892
-
-
Stevanin, G.1
Trottier, Y.2
Cancel, G.3
-
10
-
-
0027256423
-
Direct detection of novel expanded trinucleotide repeats in the human genome
-
Schalling M, Hudson TJ, Buetow KH, Housman DE. Direct detection of novel expanded trinucleotide repeats in the human genome. Nat Genet 1993;4:135-139.
-
(1993)
Nat Genet
, vol.4
, pp. 135-139
-
-
Schalling, M.1
Hudson, T.J.2
Buetow, K.H.3
Housman, D.E.4
|