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

• Autores principales: Narongsak Nakwan (Autor), Surakameth Mahasirimongkol (Autor), Nusara Satproedprai (Autor), Tassamonwan Chaiyasung (Autor), Punna Kunhapan (Autor), Cheep Charoenlap (Autor), Kamonnut Singkhamanan (Autor), Chariyawan Charalsawadi (Autor)
• Formato: Libro
• Publicado: Elsevier, 2022-07-01T00:00:00Z.
• Materias: article
• Acceso en línea: Connect to this object online.

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)...