| Literature DB >> 11914418 |
G Stevanin1, A Camuzat, S E Holmes, C Julien, R Sahloul, C Dodé, V Hahn-Barma, C A Ross, R L Margolis, A Durr, A Brice.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2002 PMID: 11914418 DOI: 10.1212/wnl.58.6.965
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910