4.7 Article

CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients

Journal

NEUROLOGY
Volume 58, Issue 6, Pages 965-967

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.58.6.965

Keywords

-

Ask authors/readers for more resources

The authors report a large series of patients with Huntington disease (HD)-like phenotype without CAG repeat expansions in the IT15 gene that were screened for the newly identified CAG/CTG expansion in the gene encoding junctophilin-3. Normal alleles in controls had from 8 to 28 repeats. A single patient of North African origin with typical HD carried an allele with 50 uninterrupted repeats, representing approximately 2% of the non-IT15 HD patients tested. Therefore, further genetic heterogeneity is expected in HD.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available