Cargando…
Discovery of Potential New Gene Variants and Inflammatory Cytokine Associations with Fibromyalgia Syndrome by Whole Exome Sequencing
Fibromyalgia syndrome (FMS) is a chronic musculoskeletal pain disorder affecting 2% to 5% of the general population. Both genetic and environmental factors may be involved. To ascertain in an unbiased manner which genes play a role in the disorder, we performed complete exome sequencing on a subset...
Autores principales: | Feng, Jinong, Zhang, Zhifang, Wu, Xiwei, Mao, Allen, Chang, Frances, Deng, Xutao, Gao, Harry, Ouyang, Ching, Dery, Kenneth J., Le, Keith, Longmate, Jeffrey, Marek, Claudia, St. Amand, R. Paul, Krontiris, Theodore G., Shively, John E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3677902/ https://www.ncbi.nlm.nih.gov/pubmed/23762283 http://dx.doi.org/10.1371/journal.pone.0065033 |
Ejemplares similares
-
Missense Mutations in the MEFV Gene Are Associated with Fibromyalgia Syndrome and Correlate with Elevated IL-1β Plasma Levels
por: Feng, Jinong, et al.
Publicado: (2009) -
SNPs in inflammatory genes CCL11, CCL4 and MEFV in a fibromyalgia family study
por: Zhang, Zhifang, et al.
Publicado: (2018) -
Three Ways of Combining Genotyping and Resequencing in Case-Control Association Studies
por: Longmate, Jeffrey A., et al.
Publicado: (2010) -
Mutation discovery in mice by whole exome sequencing
por: Fairfield, Heather, et al.
Publicado: (2011) -
Whole‐exome sequencing for variant discovery in blepharospasm
por: Tian, Jun, et al.
Publicado: (2018)