✦ LIBER ✦

Huntington disease-like 2: the first patient with apparent European ancestry

✍ Scribed by C Santos; H Wanderley; L Vedolin; SDJ Pena; L Jardim; J Sequeiros

Book ID: 110888580
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 228 KB
Volume: 73
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.2008.00981.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Huntington’s disease-like 2 and apparent

Huntington’s disease-like 2 and apparent ancestry

✍ GGR Rodrigues; HAG Teive; V Tumas 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 54 KB

A South African mixed ancestry family wi

A South African mixed ancestry family with Huntington disease-like 2: Clinical and genetic features

✍ Soraya Bardien; Fatima Abrahams; Himla Soodyall; Lize van der Merwe; Jacquie Gre 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 209 KB

## Abstract Huntington disease‐like 2 (HDL2) is a neurodegenerative disorder caused by an expansion of a CTG repeat in the junctophilin‐3 gene (__JPH3__). A limited number of HDL2 families have been reported, all of apparently Black African ancestry. We report on a South African family that present

The Huntington's disease-like syndromes:

The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test

✍ Schneider, Susanne A; Walker, Ruth H; Bhatia, Kailash P 📂 Article 📅 2007 🏛 Nature Publishing Group 🌐 English ⚖ 217 KB

A repeat expansion in the gene encoding

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

✍ Holmes, Susan E.; O'Hearn, Elizabeth; Rosenblatt, Adam; Callahan, Colleen; Hwang 📂 Article 📅 2001 🏛 Nature Publishing Group 🌐 English ⚖ 584 KB

Genetic analysis of polymorphisms in the

Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients

✍ Yu-Chun Tsai, Silke Metzger, Olaf Riess, Anne S Soehn, Huu Phuc Nguyen 📂 Article 📅 2012 🏛 BioMed Central 🌐 English ⚖ 260 KB

correction: A CTG trinucleotide repeat e

correction: A CTG trinucleotide repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease–like 2

📂 Article 📅 2002 🏛 Nature Publishing Group 🌐 English ⚖ 95 KB