Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene

Bronchopulmonary dysplasia (BPD), the main consequence of prematurity, has a significant heritability, but little is known about predisposing genes. The aim of this study was to identify gene loci predisposing infants to BPD. The initial genome-wide association study (GWAS) included 174 Finnish pret...

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Detalles Bibliográficos
Autores principales: Mahlman, Mari, Karjalainen, Minna K., Huusko, Johanna M., Andersson, Sture, Kari, M. Anneli, Tammela, Outi K. T., Sankilampi, Ulla, Lehtonen, Liisa, Marttila, Riitta H., Bassler, Dirk, Poets, Christian F., Lacaze-Masmonteil, Thierry, Danan, Claude, Delacourt, Christophe, Palotie, Aarno, Muglia, Louis J., Lavoie, Pascal M., Hadchouel, Alice, Rämet, Mika, Hallman, Mikko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571168/
https://www.ncbi.nlm.nih.gov/pubmed/28839172
http://dx.doi.org/10.1038/s41598-017-08977-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571168/
https://www.ncbi.nlm.nih.gov/pubmed/28839172
http://dx.doi.org/10.1038/s41598-017-08977-w

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