Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion

To identify genetic risk factors of childhood otitis media (OM), a genome-wide association study was performed on Finnish subjects, 829 affected children, and 2118 randomly selected controls. The most significant and validated finding was an association with an 80 kb region on chromosome 19. It incl...

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Detalles Bibliográficos
Autores principales: Einarsdottir, Elisabet, Hafrén, Lena, Leinonen, Eira, Bhutta, Mahmood F., Kentala, Erna, Kere, Juha, Mattila, Petri S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025747/
https://www.ncbi.nlm.nih.gov/pubmed/27632927
http://dx.doi.org/10.1038/srep33240

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025747/
https://www.ncbi.nlm.nih.gov/pubmed/27632927
http://dx.doi.org/10.1038/srep33240

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