Cargando…
Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes
AIM: Genome-wide association studies have identified > 30 common variants associated with Type 2 diabetes (> 5% minor allele frequency). These variants have small effects on individual risk and do not account for a large proportion of the heritable component of the disease. Monogenic forms of...
Autores principales: | Edghill, E L, Khamis, A, Weedon, M N, Walker, M, Hitman, G A, McCarthy, M I, Owen, K R, Ellard, S, T Hattersley, A, Frayling, T M |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586655/ https://www.ncbi.nlm.nih.gov/pubmed/21569088 http://dx.doi.org/10.1111/j.1464-5491.2011.03269.x |
Ejemplares similares
-
The functional "KL-VS" variant of KLOTHO is not associated with type 2 diabetes in 5028 UK Caucasians
por: Freathy, Rachel M, et al.
Publicado: (2006) -
Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency
por: De Franco, E, et al.
Publicado: (2013) -
Assessing the Combined Impact of 18 Common Genetic Variants of Modest Effect Sizes on Type 2 Diabetes Risk
por: Lango, Hana, et al.
Publicado: (2008) -
Polygenic Risk Variants for Type 2 Diabetes Susceptibility Modify Age at Diagnosis in Monogenic HNF1A Diabetes
por: Lango Allen, Hana, et al.
Publicado: (2010) -
Low Frequency Variants in the Exons Only Encoding Isoform A of HNF1A Do Not Contribute to Susceptibility to Type 2 Diabetes
por: Jafar-Mohammadi, Bahram, et al.
Publicado: (2009)