Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth

BACKGROUND: Previous studies have identified genetic variants associated with bronchopulmonary dysplasia (BPD) in extremely preterm infants. However, findings with genome-wide significance have been rare, and not replicated. We hypothesized that whole exome sequencing (WES) of premature subjects wit...

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Detalles Bibliográficos
Autores principales: Hamvas, Aaron, Feng, Rui, Bi, Yingtao, Wang, Fan, Bhattacharya, Soumyaroop, Mereness, Jared, Kaushal, Madhurima, Cotten, C Michael, Ballard, Philip L, Mariani, Thomas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195962/
https://www.ncbi.nlm.nih.gov/pubmed/30342483
http://dx.doi.org/10.1186/s12863-018-0679-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195962/
https://www.ncbi.nlm.nih.gov/pubmed/30342483
http://dx.doi.org/10.1186/s12863-018-0679-7

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