Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype

被引：20

作者：

Bauer, I ^{[1
]}

Gencik, M

Laccone, F

Peters, H

Weber, BHF

Feder, EH

Weirich, H

Morris-Rosendahl, DJ

Rolfs, A

Gencikova, A

Bauer, P

Wenning, GK

Epplen, JT

Holmes, SE

Margolis, RL

Ross, CA

Riess, O

机构：

[1] Univ Rostock, Dept Med Genet, Rostock, Germany

[2] Ruhr Univ Bochum, Dept Human Mol Genet, D-4630 Bochum, Germany

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

[4] Humboldt Univ, Charite, Dept Med Genet, Berlin, Germany

[5] Univ Wurzburg, Inst Human Genet, Wurzburg, Germany

[6] Univ Freiburg, Inst Human Genet & Anthropol, Freiburg, Germany

[7] Med Genet Zentrum, Munich, Germany

[8] Univ Rostock, Dept Neurol, Rostock, Germany

[9] Univ Tubingen, Dept Med Genet, Tubingen, Germany

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

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

[12] Johns Hopkins Univ, Sch Med, Program Cellular & Mol Med, Baltimore, MD USA

[13] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD USA

来源：

ANNALS OF NEUROLOGY | 2002年 / 51卷 / 05期

关键词：

D O I：

10.1002/ana.10184

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：662 / 662

页数：1

共 4 条

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[4] A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion [J].

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