Trinucleotide repeat expansions in thejunctophilin-3 gene are not found in caucasian patients with a huntington's disease-like phenotype-Reference-Cited by-同舟云学术

Trinucleotide repeat expansions in thejunctophilin-3 gene are not found in caucasian patients with a huntington's disease-like phenotype

Published:2002-04-30 Issue:5 Volume:51 Page:662-662
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Bauer Ingrid,Gencik Martin,Laccone Franco,Peters Hartmut,Weber Bernhard H. F.,Feder Elke Holinski,Weirich Helga,Morris-Rosendahl Deborah J.,Rolfs Arndt,Gencikova Alexandra,Bauer Peter,Wenning Gregor K.,Epplen J�rg T.,Holmes Susan E.,Margolis Russell L.,Ross Christopher A.,Riess Olaf

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference4 articles.

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

2. A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion

3. A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease–like 2

4. DNA analysis of Huntington’s disease

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