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, Surakameth Mahasirimongkol, Nusara Satproedprai, Tassamonwan Chaiyasung, Punna Kunhapan, Cheep Charoenlap, Kamonnut Singkhamanan, Chariyawan Charalsawadi
Format: Article
Language:English
Published: Elsevier 2022-07-01
Series:Jornal de Pediatria
Subjects:
PPHN
Polymorphism
SNP
EPAS1 gene
Association study
Online Access:http://www.sciencedirect.com/science/article/pii/S0021755721001376

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http://www.sciencedirect.com/science/article/pii/S0021755721001376

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