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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:PLoS One
मुख्य लेखकों: 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.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Public Library of Science 2017
विषय:
ऑनलाइन पहुंच: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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