-
1
-
-
0035852807
-
Autosomal dominant spinocerebellar ataxias ad infinitum?
-
Subramony SH, Filla A. Autosomal dominant spinocerebellar ataxias ad infinitum? Neurology 2001;56:287-289.
-
(2001)
Neurology
, vol.56
, pp. 287-289
-
-
Subramony, S.H.1
Filla, A.2
-
2
-
-
0038048459
-
Spinocerebellar ataxia 15 (SCA15) maps to 3p24.2-3pter; exclusion of the ITPR1 gene, the human orthologue of an ataxia mouse mutant
-
Melanie AK, Marina LK, et al. Spinocerebellar ataxia 15 (SCA15) maps to 3p24.2-3pter; exclusion of the ITPR1 gene, the human orthologue of an ataxia mouse mutant. Neurobiol Dis 2003;13:147-157.
-
(2003)
Neurobiol Dis
, vol.13
, pp. 147-157
-
-
Melanie, A.K.1
Marina, L.K.2
-
3
-
-
0035393427
-
SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
-
Nakamura K, Jeong SY, Uchihara T, et al. SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein. Hum Mol Genet 2001;10:1441-1448.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1441-1448
-
-
Nakamura, K.1
Jeong, S.Y.2
Uchihara, T.3
-
4
-
-
0036820509
-
Identification of a novel SCA locus (SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21
-
Verbeek DS, Schelhaas JH, Ippel EF, et al. Identification of a novel SCA locus (SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21. Hum Genet 2002;111:388-393.
-
(2002)
Hum Genet
, vol.111
, pp. 388-393
-
-
Verbeek, D.S.1
Schelhaas, J.H.2
Ippel, E.F.3
-
5
-
-
0036830123
-
A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7q21.3-p15.1
-
Vuuillaume I, Devos D, Schraen-Maschke S, et al. A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7q21.3-p15.1. Ann Neurol 2002;52:666-670.
-
(2002)
Ann Neurol
, vol.52
, pp. 666-670
-
-
Vuuillaume, I.1
Devos, D.2
Schraen-Maschke, S.3
-
6
-
-
0037677603
-
A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23
-
Chung M-Y, Lu Y-C, Cheng N-C, et al. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23. Brain 2003;126:1293-1299.
-
(2003)
Brain
, vol.126
, pp. 1293-1299
-
-
Chung, M.-Y.1
Lu, Y.-C.2
Cheng, N.-C.3
-
7
-
-
1342311033
-
A new syndrome of hereditary sensory and cerebellar ataxia with muscle atrophy, SCA18: Linkage to chromosome 7q31-7q32
-
Brkanac Z, Fernandez M, Matsushita M, et al. A new syndrome of hereditary sensory and cerebellar ataxia with muscle atrophy, SCA18: linkage to chromosome 7q31-7q32. Am J Hum Genet 2001;69(suppl): 497.
-
(2001)
Am J Hum Genet
, vol.69
, Issue.SUPPL.
, pp. 497
-
-
Brkanac, Z.1
Fernandez, M.2
Matsushita, M.3
-
8
-
-
0032231668
-
Close association between prevalences of dominantly inherited SCAs with CAG repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations
-
Takano H, Cancel G, Ikeuchi T, et al. Close association between prevalences of dominantly inherited SCAs with CAG repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. Am J Hum Genet 1998;63:1060-1066.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1060-1066
-
-
Takano, H.1
Cancel, G.2
Ikeuchi, T.3
-
9
-
-
0034098774
-
Allegro, a new computer program for multipoint linkage analysis
-
Gudbjartsson DF, Jonasson K, Frigge ML, Kong A. Allegro, a new computer program for multipoint linkage analysis. Nat Genet 2000;25:12-13.
-
(2000)
Nat Genet
, vol.25
, pp. 12-13
-
-
Gudbjartsson, D.F.1
Jonasson, K.2
Frigge, M.L.3
Kong, A.4
-
10
-
-
0035960565
-
A new autosomal dominant pure cerebellar ataxia
-
Storey E, Gardner RJM, Knight MA, et al. A new autosomal dominant pure cerebellar ataxia. Neurol 2001;57:1913-1915.
-
(2001)
Neurol
, vol.57
, pp. 1913-1915
-
-
Storey, E.1
Gardner, R.J.M.2
Knight, M.A.3
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