Cargando…
Huntington's disease: the case for genetic modifiers
For almost three decades, Huntington's disease has been a prototype for the application of genetic strategies to human disease. HD, the Huntington's disease gene, was the first autosomal defect mapped using only DNA markers, a finding in 1983 that helped to spur similar studies in many oth...
Autores principales: | Gusella, James F, MacDonald, Marcy E |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768966/ https://www.ncbi.nlm.nih.gov/pubmed/19725930 http://dx.doi.org/10.1186/gm80 |
Ejemplares similares
-
Genetic analysis of the GRIK2 modifier effect in Huntington's disease
por: Zeng, Wenqi, et al.
Publicado: (2006) -
Huntington’s Disease Pathogenesis: Two Sequential Components
por: Hong, Eun Pyo, et al.
Publicado: (2021) -
Population-specific genetic modification of Huntington's disease in Venezuela
por: Chao, Michael J., et al.
Publicado: (2018) -
Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease
por: McAllister, Branduff, et al.
Publicado: (2021) -
Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1
por: Lobanov, Sergey V., et al.
Publicado: (2022)