Cargando…
Genetic analysis of the GRIK2 modifier effect in Huntington's disease
BACKGROUND: In Huntington's disease (HD), age at neurological onset is inversely correlated with the length of the CAG trinucleotide repeat mutation, but can be modified by genetic factors beyond the HD gene. Association of a relatively infrequent 16 TAA allele of a trinucleotide repeat polymor...
Autores principales: | Zeng, Wenqi, Gillis, Tammy, Hakky, Michael, Djoussé, Luc, Myers, Richard H, MacDonald, Marcy E, Gusella, James F |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1618398/ https://www.ncbi.nlm.nih.gov/pubmed/16959037 http://dx.doi.org/10.1186/1471-2202-7-62 |
Ejemplares similares
-
Huntington's disease: the case for genetic modifiers
por: Gusella, James F, et al.
Publicado: (2009) -
Chromosome substitution strain assessment of a Huntington’s disease modifier locus
por: Ramos, Eliana Marisa, et al.
Publicado: (2015) -
Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease
por: Ramos, Eliana Marisa, et al.
Publicado: (2015) -
Kainate receptor subunit 1 (GRIK1) risk variants and GRIK1 deficiency were detected in the Indian ADHD probands
por: Chatterjee, Mahasweta, et al.
Publicado: (2022) -
Population-specific genetic modification of Huntington's disease in Venezuela
por: Chao, Michael J., et al.
Publicado: (2018)