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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Sci Rep
Prif Awduron: Einarsdottir, Elisabet, Hafrén, Lena, Leinonen, Eira, Bhutta, Mahmood F., Kentala, Erna, Kere, Juha, Mattila, Petri S.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2016
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5025747/
https://ncbi.nlm.nih.gov/pubmed/27632927
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep33240
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