Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study

Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study

Objective: To explore possible genes related to the development of persistent pulmonary hypertension of the newborn (PPHN). Methods: The authors identified 285 single nucleotide polymorphisms (SNPs) of 11 candidate genes (BMPR2, EPAS1, PDE3A, VEGFA, ENG, NOTCH3, SOD3, CPS1, ABCA3, ACVRL1, and SMAD9)...

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Main Authors: Narongsak Nakwan (Author), Surakameth Mahasirimongkol (Author), Nusara Satproedprai (Author), Tassamonwan Chaiyasung (Author), Punna Kunhapan (Author), Cheep Charoenlap (Author), Kamonnut Singkhamanan (Author), Chariyawan Charalsawadi (Author)
Format: Book
Published: Elsevier, 2022-07-01T00:00:00Z.
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