A novel TCF7L2 type 2 diabetes SNP identified from fine mapping in African American women

SNP rs7903146 in the Wnt pathway’s TCF7L2 gene is the variant most significantly associated with type 2 diabetes to date, with associations observed across diverse populations. We sought to determine whether variants in other Wnt pathway genes are also associated with this disease. We evaluated 69 g...

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Detalles Bibliográficos
Autores principales: Haddad, Stephen A., Palmer, Julie R., Lunetta, Kathryn L., Ng, Maggie C. Y., Ruiz-Narváez, Edward A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333820/
https://www.ncbi.nlm.nih.gov/pubmed/28253288
http://dx.doi.org/10.1371/journal.pone.0172577

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333820/
https://www.ncbi.nlm.nih.gov/pubmed/28253288
http://dx.doi.org/10.1371/journal.pone.0172577

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