Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

Preterm birth is a leading cause of morbidity and mortality in infants. Genetic and environmental factors play a role in the susceptibility to preterm birth, but despite many investigations, the genetic basis for preterm birth remain largely unknown. Our objective was to identify rare, possibly dama...

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Publicat a:PLoS Genet
Autors principals: Huusko, Johanna M., Karjalainen, Minna K., Graham, Britney E., Zhang, Ge, Farrow, Emily G., Miller, Neil A., Jacobsson, Bo, Eidem, Haley R., Murray, Jeffrey C., Bedell, Bruce, Breheny, Patrick, Brown, Noah W., Bødker, Frans L., Litterman, Nadia K., Jiang, Pan-Pan, Russell, Laura, Hinds, David A., Hu, Youna, Rokas, Antonis, Teramo, Kari, Christensen, Kaare, Williams, Scott M., Rämet, Mika, Kingsmore, Stephen F., Ryckman, Kelli K., Hallman, Mikko, Muglia, Louis J.
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2018
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6042692/
https://ncbi.nlm.nih.gov/pubmed/30001343
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1007394
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