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

• 主要な著者: Narongsak Nakwan (著者), Surakameth Mahasirimongkol (著者), Nusara Satproedprai (著者), Tassamonwan Chaiyasung (著者), Punna Kunhapan (著者), Cheep Charoenlap (著者), Kamonnut Singkhamanan (著者), Chariyawan Charalsawadi (著者)
• フォーマット: 図書
• 出版事項: Elsevier, 2022-07-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: 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)...