Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype

被引：69

作者：

Bauer, P

Laccone, F

Rolfs, A

Wüllner, U

Bösch, S

Peters, H

Liebscher, S

Scheible, M

Epplen, JT

Weber, BHF

Holinski-Feder, E

Weirich-Schwaiger, H

Morris-Rosendahl, DJ

Andrich, J

Riess, O

机构：

[1] Univ Tubingen, Dept Med Genet, D-72076 Tubingen, Germany

[2] Univ Gottingen, Dept Human Genet, D-3400 Gottingen, Germany

[3] Univ Rostock, Dept Neurol, D-2500 Rostock 1, Germany

[4] Univ Bonn, Dept Neurol, D-5300 Bonn, Germany

[5] Univ Innsbruck, Dept Neurol, A-6020 Innsbruck, Austria

[6] Humboldt Univ, Charite, Dept Med Genet, D-1086 Berlin, Germany

[7] Ruhr Univ Bochum, Dept Human Genet, Bochum, Germany

[8] Univ Wurzburg, Inst Human Genet, D-97070 Wurzburg, Germany

[9] Med Genet Zentrum, Munich, Germany

[10] Univ Innsbruck, Inst Med Biol & Human Genet, A-6020 Innsbruck, Austria

[11] Univ Freiburg, Inst Human Genet & Anthropol, D-7800 Freiburg, Germany

[12] Ruhr Univ Bochum, Dept Neurol, Bochum, Germany

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 03期

关键词：

D O I：

10.1136/jmg.2003.015602

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：230 / 232

页数：3

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