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Rare mutations and potentially damaging missense variants in genes encoding fibrillar collagens and proteins involved in their production are candidates for risk for preterm premature rupture of membranes

Preterm premature rupture of membranes (PPROM) is the leading identifiable cause of preterm birth with ~ 40% of preterm births being associated with PPROM and occurs in 1% - 2% of all pregnancies. We hypothesized that multiple rare variants in fetal genes involved in extracellular matrix synthesis w...

Szczegółowa specyfikacja

Zapisane w:
Opis bibliograficzny
Wydane w:PLoS One
Główni autorzy: Modi, Bhavi P., Teves, Maria E., Pearson, Laurel N., Parikh, Hardik I., Chaemsaithong, Piya, Sheth, Nihar U., York, Timothy P., Romero, Roberto, Strauss, Jerome F.
Format: Artigo
Język:Inglês
Wydane: Public Library of Science 2017
Hasła przedmiotowe:
Dostęp online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5367779/
https://ncbi.nlm.nih.gov/pubmed/28346524
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0174356
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