-
1
-
-
0028260436
-
Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded CAG repeat
-
Ambrose, C.M., Duyao, M.P., Barnes, G., Bates, G.P., Lin, C.S., Srinidhi, J., Baxendale, S., Hummerich, H., Lehrach, H., Altherr, M., Wasmuth, J., Buckler, A., Church, D., Housman, D., Berks, M., Micklem, G., Durbin, R., Dodge, A., Read, A., Gusella, J. and MacDonald, M.E., Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded CAG repeat, Somat. Cell Mol. Genet., 20 (1994) 27-38.
-
(1994)
Somat. Cell Mol. Genet.
, vol.20
, pp. 27-38
-
-
Ambrose, C.M.1
Duyao, M.P.2
Barnes, G.3
Bates, G.P.4
Lin, C.S.5
Srinidhi, J.6
Baxendale, S.7
Hummerich, H.8
Lehrach, H.9
Altherr, M.10
Wasmuth, J.11
Buckler, A.12
Church, D.13
Housman, D.14
Berks, M.15
Micklem, G.16
Durbin, R.17
Dodge, A.18
Read, A.19
Gusella, J.20
MacDonald, M.E.21
more..
-
2
-
-
0026772992
-
Spatial and temporal expression of α and β thyroid hormone receptor mRNAs, including the β2 subtype, in the developing mammalian nervous system
-
Bradley, D.J., Towle, H.C. and Young, W.S.III, Spatial and temporal expression of α and β thyroid hormone receptor mRNAs, including the β2 subtype, in the developing mammalian nervous system, J. Neurosci., 12 (1992) 2288-2302.
-
(1992)
J. Neurosci.
, vol.12
, pp. 2288-2302
-
-
Bradley, D.J.1
Towle, H.C.2
Young W.S. III3
-
3
-
-
0029163222
-
SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat
-
Burright, E.N., Clark, H.B., Servadio, A., Matilla, T., Feddersen, R.M., Yunis, W.S., Duvick, L.A., Zoghbi, H.Y., Orr, H.T., SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat, Cell, 82 (1995) 937-948.
-
(1995)
Cell
, vol.82
, pp. 937-948
-
-
Burright, E.N.1
Clark, H.B.2
Servadio, A.3
Matilla, T.4
Feddersen, R.M.5
Yunis, W.S.6
Duvick, L.A.7
Zoghbi, H.Y.8
Orr, H.T.9
-
4
-
-
0004135663
-
-
Elsevier, New York
-
Davis, L.G., Dibner, M.D. and Battey, J.F., Basic Methods in Molecular Biology, Elsevier, New York, 1986,
-
(1986)
Basic Methods in Molecular Biology
-
-
Davis, L.G.1
Dibner, M.D.2
Battey, J.F.3
-
5
-
-
0029082383
-
Inactivation of the mouse Huntington's disease gene homolog hdh
-
Duyao, M.P., Auerbach, A.B., Ryan, A., Persichetti, Barnes, G.T., McNeil, S.M., Ge, P., Vonsattel, J-P., Gusella, J.F., Joyner, A.L., and MacDonald, M.E. Inactivation of the mouse Huntington's disease gene homolog hdh, Science, 269 (1995) 407-410.
-
(1995)
Science
, vol.269
, pp. 407-410
-
-
Duyao, M.P.1
Auerbach, A.B.2
Ryan, A.3
Persichetti4
Barnes, G.T.5
McNeil, S.M.6
Ge, P.7
Vonsattel, J.-P.8
Gusella, J.F.9
Joyner, A.L.10
MacDonald, M.E.11
-
6
-
-
0027507667
-
Human genetic diseases due to condon reiteration: Relationship to an evolutionary mechanism
-
Green, H., Human genetic diseases due to condon reiteration: Relationship to an evolutionary mechanism, Cell, 74 (1993) 955-956.
-
(1993)
Cell
, vol.74
, pp. 955-956
-
-
Green, H.1
-
7
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
Huntington's Disease Collaborative Research Group, A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes, Cell, 72 (1993) 971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
8
-
-
85047678013
-
Denatao-rubro-pallidoluysian atrophy: A clinico-pathological study
-
Iizuka, R., Hirayama, K., and Maehara, K. Denatao-rubro-pallidoluysian atrophy: a clinico-pathological study, J. Neurol. Neurosurg. Psychiatry, 47 (1984) 1288-1298.
-
(1984)
J. Neurol. Neurosurg. Psychiatry
, vol.47
, pp. 1288-1298
-
-
Iizuka, R.1
Hirayama, K.2
Maehara, K.3
-
9
-
-
0028143527
-
CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1
-
Kawaguchi, Y., Okamoto, T., Taniwaki, T., Aizawa, M., Inoue, M., Katayama, S., Kawakami, H., Nakamura, S., Nishimura, M., Akiguchi, I., Kimura, J., Narumiya, S. and Kakizuka, A., CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1, Nature Genet., 8 (1994) 221-228.
-
(1994)
Nature Genet.
, vol.8
, pp. 221-228
-
-
Kawaguchi, Y.1
Okamoto, T.2
Taniwaki, T.3
Aizawa, M.4
Inoue, M.5
Katayama, S.6
Kawakami, H.7
Nakamura, S.8
Nishimura, M.9
Akiguchi, I.10
Kimura, J.11
Narumiya, S.12
Kakizuka, A.13
-
10
-
-
0028216760
-
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
-
Koide, R., Ikeuchi, T., Onodera, O., Tanaka, H., Igarashi, S., Endo, K., Takahashi, H., Kondo, R., Ishikawa, A., Hayashi, T., Saito, M., Tomoda, A., Miike, T., Naito, H., Ikuta, F. and Tsuji, S., Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA), Nature Genet., 6 (1994) 9-13.
-
(1994)
Nature Genet.
, vol.6
, pp. 9-13
-
-
Koide, R.1
Ikeuchi, T.2
Onodera, O.3
Tanaka, H.4
Igarashi, S.5
Endo, K.6
Takahashi, H.7
Kondo, R.8
Ishikawa, A.9
Hayashi, T.10
Saito, M.11
Tomoda, A.12
Miike, T.13
Naito, H.14
Ikuta, F.15
Tsuji, S.16
-
11
-
-
0028080406
-
Trinucleotide repeat expansion in neurological disease
-
La Spada, A.R., Paulson, H.L. and Fischbeck, K.H., Trinucleotide repeat expansion in neurological disease, Ann. Neurol., 36 (1994) 814-822.
-
(1994)
Ann. Neurol.
, vol.36
, pp. 814-822
-
-
La Spada, A.R.1
Paulson, H.L.2
Fischbeck, K.H.3
-
12
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada, A.R., Wilson, E.M., Lubahn, D.B., Harding, A.E. and Fischbeck, K.H., Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy, Nature, 352 (1991) 77-79.
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
13
-
-
0343927697
-
Expression of mRNA for DRPLA gene (atrophin-1) and HD gene (IT15) in developmental and adult brain
-
Li, S-H., Margolis, R.L., Li, X-J. and Ross, C.A., Expression of mRNA for DRPLA gene (atrophin-1) and HD gene (IT15) in developmental and adult brain, Neurosci. Abstr., 24 (1994) 1648.
-
(1994)
Neurosci. Abstr.
, vol.24
, pp. 1648
-
-
Li, S.-H.1
Margolis, R.L.2
Li, X.-J.3
Ross, C.A.4
-
14
-
-
0027297703
-
Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms
-
Li, S-H., Mclnnis, M.G., Margolis, R.L., Antonarakis, S.E. and Ross, C.A., Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms, Genomics, 16 (1993) 572-579.
-
(1993)
Genomics
, vol.16
, pp. 572-579
-
-
Li, S.-H.1
McLnnis, M.G.2
Margolis, R.L.3
Antonarakis, S.E.4
Ross, C.A.5
-
15
-
-
0027484673
-
Huntington's disease gene (IT15) is widely expressed in human and rat tissues
-
Li, S-H., Schilling, G., Young, W.S. III, Li, X-J., Margolis, R.L., Stine, O.C., Wagster, M.V., Abbott, M.H., Franz, M.L., Ranen, N.G., Folstein, S.E., Hedreen, J.C. and Ross, C.A., Huntington's disease gene (IT15) is widely expressed in human and rat tissues, Neuron, 11 (1993) 985-993.
-
(1993)
Neuron
, vol.11
, pp. 985-993
-
-
Li, S.-H.1
Schilling, G.2
Young W.S. III3
Li, X.-J.4
Margolis, R.L.5
Stine, O.C.6
Wagster, M.V.7
Abbott, M.H.8
Franz, M.L.9
Ranen, N.G.10
Folstein, S.E.11
Hedreen, J.C.12
Ross, C.A.13
-
16
-
-
0024306555
-
Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity
-
Lubahn, D.B., Brown, T.R., Simental, J.A., Higgs, H.N., Migeon, C.J., Wilson, E.M. and French, F.S., Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity, Proc. Natl. Acad. Sci. USA, 86 (1989) 9534-9538.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 9534-9538
-
-
Lubahn, D.B.1
Brown, T.R.2
Simental, J.A.3
Higgs, H.N.4
Migeon, C.J.5
Wilson, E.M.6
French, F.S.7
-
17
-
-
0028843242
-
Abnormal androgen receptor binding affinity in subjects with Kennedy's disease (spinal and bulbar muscular atropy)
-
MacLean, H.E., Choi, W-T., Rekaris, G., Warne, G.L. and Zajac, J.D., Abnormal androgen receptor binding affinity in subjects with Kennedy's disease (spinal and bulbar muscular atropy), J. Clin. Endocrinol. Metab., 80 (1995) 508-516.
-
(1995)
J. Clin. Endocrinol. Metab.
, vol.80
, pp. 508-516
-
-
MacLean, H.E.1
Choi, W.-T.2
Rekaris, G.3
Warne, G.L.4
Zajac, J.D.5
-
18
-
-
0026550512
-
Molecular characterization of a novel rat protein structurally related to poly(A) binding protein and the 70K protein of the U1 small nuclear ribonucleoprotein particle (snRNP)
-
Mueller, D, Rehbein, M., Baumeister, H., Richter, D., Molecular characterization of a novel rat protein structurally related to poly(A) binding protein and the 70K protein of the U1 small nuclear ribonucleoprotein particle (snRNP), Nucleic Acid Res., 20 (1992) 1471-1475.
-
(1992)
Nucleic Acid Res.
, vol.20
, pp. 1471-1475
-
-
Mueller, D.1
Rehbein, M.2
Baumeister, H.3
Richter, D.4
-
19
-
-
0024432090
-
Homozygote for Huntington's disease
-
Myers, R.H., Leavitt, J., Farrer, L.A., Jagadeesh, J., McFarlane, H., Mastromauro, C.A., Mark, R.J. and Gusella, J.F., Homozygote for Huntington's disease, Am. J. Hum. Genet., 45 (1989) 615-618.
-
(1989)
Am. J. Hum. Genet.
, vol.45
, pp. 615-618
-
-
Myers, R.H.1
Leavitt, J.2
Farrer, L.A.3
Jagadeesh, J.4
McFarlane, H.5
Mastromauro, C.A.6
Mark, R.J.7
Gusella, J.F.8
-
20
-
-
0028060244
-
Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)
-
Nagafuchi, S., Yanagisawa, H., Ohsaki, E., Shirayama, T., Tadokoro, K., Inoue, T. and Yamada, M., Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA), Nature Genet., 8 (1994) 177-182.
-
(1994)
Nature Genet.
, vol.8
, pp. 177-182
-
-
Nagafuchi, S.1
Yanagisawa, H.2
Ohsaki, E.3
Shirayama, T.4
Tadokoro, K.5
Inoue, T.6
Yamada, M.7
-
21
-
-
0028335386
-
Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12 p
-
Nagafuchi, S., Yanagisawa, H., Sato, K., Shirayama, T., Ohsaki, E., Bundo, M., Takeda, T., Tadokoro, K., Kondo, I., Murayama, N., Tanaka, Y., Kikushima, H., Umino, K., Kurosawa, H., Furukawa, T., Nihei, K., Inoue, T., Sano, A., Komure, O., Takahashi, M., Yoshizawa, T., Kanazawa, I. and Yamada, M., Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12 p, Nature Genet., 6 (1994) 14-18.
-
(1994)
Nature Genet.
, vol.6
, pp. 14-18
-
-
Nagafuchi, S.1
Yanagisawa, H.2
Sato, K.3
Shirayama, T.4
Ohsaki, E.5
Bundo, M.6
Takeda, T.7
Tadokoro, K.8
Kondo, I.9
Murayama, N.10
Tanaka, Y.11
Kikushima, H.12
Umino, K.13
Kurosawa, H.14
Furukawa, T.15
Nihei, K.16
Inoue, T.17
Sano, A.18
Komure, O.19
Takahashi, M.20
Yoshizawa, T.21
Kanazawa, I.22
Yamada, M.23
more..
-
22
-
-
0020064620
-
Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy
-
Naito, H. and Oyanagi, S., Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy, Neurology, 32 (1982) 798-807.
-
(1982)
Neurology
, vol.32
, pp. 798-807
-
-
Naito, H.1
Oyanagi, S.2
-
23
-
-
0029055717
-
Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes
-
Nassir, J., Floresco, S.B., O'Kuskey, J.R., Diewert, V.M., Richman, J.M., Zeisler, J., Borowski, A., Marth, J.D., Phillips, A.G., and Hayden, M.R., Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes, Cell, 81 (1995) 1-20.
-
(1995)
Cell
, vol.81
, pp. 1-20
-
-
Nassir, J.1
Floresco, S.B.2
O'Kuskey, J.R.3
Diewert, V.M.4
Richman, J.M.5
Zeisler, J.6
Borowski, A.7
Marth, J.D.8
Phillips, A.G.9
Hayden, M.R.10
-
24
-
-
0027164698
-
Expansion of an unstable CAG repeat in spinocerebellar ataxia type 1
-
Orr, H.T., Chung, M.-Y., Banfi, S., Kwiatkowski, T.J.Jr., Servadio, A., Beaudet, A.L., McCall, A.E., Duvick, L.A., Ranum, L.P.W. and Zoghbi, H.Y., Expansion of an unstable CAG repeat in spinocerebellar ataxia type 1, Nature Genet., 4 (1993) 221-226.
-
(1993)
Nature Genet.
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.-Y.2
Banfi, S.3
Kwiatkowski T.J., Jr.4
Servadio, A.5
Beaudet, A.L.6
McCall, A.E.7
Duvick, L.A.8
Ranum, L.P.W.9
Zoghbi, H.Y.10
-
25
-
-
0022322597
-
Design and characterization of peptides with amphiphilic B-strand structures
-
Osterman, D.G., and Kaiser, E.T., Design and characterization of peptides with amphiphilic B-strand structures, J Cell. Biochem., 29 (1985) 57-72.
-
(1985)
J Cell. Biochem.
, vol.29
, pp. 57-72
-
-
Osterman, D.G.1
Kaiser, E.T.2
-
26
-
-
0027988041
-
Polar zippers: Their role in human disease
-
Perutz, M., Polar zippers: Their role in human disease, Protein Sci., 3 (1995) 1629-1637.
-
(1995)
Protein Sci.
, vol.3
, pp. 1629-1637
-
-
Perutz, M.1
-
27
-
-
0027300219
-
Genes with triplet repeats: Candidate mediators of neuropsychiatric disorders
-
Ross, C.A., Mclnnis, M.G., Margolis, R.L. and Li, S-H., Genes with triplet repeats: Candidate mediators of neuropsychiatric disorders, Trends Neurosci., 16 (1993) 254-260.
-
(1993)
Trends Neurosci.
, vol.16
, pp. 254-260
-
-
Ross, C.A.1
McLnnis, M.G.2
Margolis, R.L.3
Li, S.-H.4
-
28
-
-
33744887360
-
When more is less: Pathogenesis of glutamine repeat neurodegenerative diseases
-
in press
-
Ross, C.A., When more is less: Pathogenesis of glutamine repeat neurodegenerative diseases, Neuron, in press.
-
Neuron
-
-
Ross, C.A.1
-
29
-
-
0029092340
-
Expression of Huntington's disease (IT15) protein product in HD patients
-
Schilling, G., Sharp, A.H., Loev, S.J., Wagster, M.V., Li, S-H., Stine, O.C., and Ross, C.A., Expression of Huntington's disease (IT15) protein product in HD patients, Hum. Mol. Genet., 4 (1995) 1365-1371.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1365-1371
-
-
Schilling, G.1
Sharp, A.H.2
Loev, S.J.3
Wagster, M.V.4
Li, S.-H.5
Stine, O.C.6
Ross, C.A.7
-
30
-
-
0029014180
-
Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals
-
Servadio, A., Koshy, B., Armstrong, D., Antalffy, B., Orr, H.T. and Zoghbi, H.Y., Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals, Nature Genet., 10 (1995) 94-98.
-
(1995)
Nature Genet.
, vol.10
, pp. 94-98
-
-
Servadio, A.1
Koshy, B.2
Armstrong, D.3
Antalffy, B.4
Orr, H.T.5
Zoghbi, H.Y.6
-
31
-
-
0029034511
-
Widespread expression of Huntingon's disease gene (IT-15) protein product
-
Sharp, A.M., Loev, S.J., Schilling, G., Li, S-H., Li, X-J., Bao, J., Wagster, M.V., Kotzuk, J.A., Steiner, J.P., Lo, A., Hedreen, J., Sisodia, S., Snyder, S.H., Dawson, T.M., Ryugo, D.K. and Ross, C.A., Widespread expression of Huntingon's disease gene (IT-15) protein product, Neuron, 14 (1995) 1-20.
-
(1995)
Neuron
, vol.14
, pp. 1-20
-
-
Sharp, A.M.1
Loev, S.J.2
Schilling, G.3
Li, S.-H.4
Li, X.-J.5
Bao, J.6
Wagster, M.V.7
Kotzuk, J.A.8
Steiner, J.P.9
Lo, A.10
Hedreen, J.11
Sisodia, S.12
Snyder, S.H.13
Dawson, T.M.14
Ryugo, D.K.15
Ross, C.A.16
-
32
-
-
0001294843
-
Unusual form of cerebellar ataxia: Combined dentato-rubral and pallido-Luysian degeneration
-
Smith, J.K., Gonda, V.E. and Malamud, N., Unusual form of cerebellar ataxia: Combined dentato-rubral and pallido-Luysian degeneration, Neurology, 8 (1958) 205-209.
-
(1958)
Neurology
, vol.8
, pp. 205-209
-
-
Smith, J.K.1
Gonda, V.E.2
Malamud, N.3
-
33
-
-
0024825955
-
Structure of the human RD gene: A highly conserved gene in the class III region of the major histocompatability complex
-
Speiser, P.W., White, P.C., Structure of the human RD gene: A highly conserved gene in the class III region of the major histocompatability complex, DNA, 8 (1989) 745-751.
-
(1989)
DNA
, vol.8
, pp. 745-751
-
-
Speiser, P.W.1
White, P.C.2
-
34
-
-
0028997643
-
Simple tandem DNA repeats and human genetic disease
-
Sutherland, G.R. and Richards, R.I., Simple tandem DNA repeats and human genetic disease, Proc. Natl. Acad. Sci. USA, 92 (1995) 3636-3641.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 3636-3641
-
-
Sutherland, G.R.1
Richards, R.I.2
-
35
-
-
0023680089
-
Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family
-
Takahashi, H., Ohama, E., Naito, H., Takeda, S., Nakashima, S., Makifuchi, T., and Ikuta, F., Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family, Neurology, 38 (1988) 1065-1070
-
(1988)
Neurology
, vol.38
, pp. 1065-1070
-
-
Takahashi, H.1
Ohama, E.2
Naito, H.3
Takeda, S.4
Nakashima, S.5
Makifuchi, T.6
Ikuta, F.7
-
36
-
-
0029055601
-
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form
-
Trottier, Y., Devys, D., Imbert, G., Saudou, F., An, I., Lutz, Y., Weber, C., Agid, Y., Hirsch, E.C. and Mandel, J-L., Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form, Nature Genet., 10 (1995) 104-110.
-
(1995)
Nature Genet.
, vol.10
, pp. 104-110
-
-
Trottier, Y.1
Devys, D.2
Imbert, G.3
Saudou, F.4
An, I.5
Lutz, Y.6
Weber, C.7
Agid, Y.8
Hirsch, E.C.9
Mandel, J.-L.10
-
37
-
-
0022780331
-
The nucleotide sequence of the fission yeast DNA toposiomerase II gene: Sturctural and functional relationships to other DNA topoisomerases
-
Uemura, T., Morikawa, K., and Yanagida, M., The nucleotide sequence of the fission yeast DNA toposiomerase II gene: sturctural and functional relationships to other DNA topoisomerases, EMBO J., 5 (1986) 2355-2361.
-
(1986)
EMBO J.
, vol.5
, pp. 2355-2361
-
-
Uemura, T.1
Morikawa, K.2
Yanagida, M.3
-
38
-
-
0023115076
-
Homozygotes for Huntington's disease
-
Wexler, N.S., Young, A.B., Tanzi, R.E., Travers, H., Starosta-Rubenstein, S., Penney, J.B., Snodgrass, S.R., Shoulson, I., Gomez, F. and Ramos-Arroyo, M.A., Homozygotes for Huntington's disease, Nature, 326 (1987) 194-197.
-
(1987)
Nature
, vol.326
, pp. 194-197
-
-
Wexler, N.S.1
Young, A.B.2
Tanzi, R.E.3
Travers, H.4
Starosta-Rubenstein, S.5
Penney, J.B.6
Snodgrass, S.R.7
Shoulson, I.8
Gomez, F.9
Ramos-Arroyo, M.A.10
-
39
-
-
0029015557
-
Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain
-
Yazawa, I., Nukina, N., Hashida, H., Goto, J., Yamada, M. and Kanazawa, I., Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain, Nature Genet., 10 (1995) 99-103.
-
(1995)
Nature Genet.
, vol.10
, pp. 99-103
-
-
Yazawa, I.1
Nukina, N.2
Hashida, H.3
Goto, J.4
Yamada, M.5
Kanazawa, I.6
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