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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Detalles Bibliográficos
Autores principales: Nakwan, Narongsak, Mahasirimongkol, Surakameth, Satproedprai, Nusara, Chaiyasung, Tassamonwan, Kunhapan, Punna, Charoenlap, Cheep, Singkhamanan, Kamonnut, Charalsawadi, Chariyawan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432230/
https://www.ncbi.nlm.nih.gov/pubmed/34678164
http://dx.doi.org/10.1016/j.jped.2021.09.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432230/
https://www.ncbi.nlm.nih.gov/pubmed/34678164
http://dx.doi.org/10.1016/j.jped.2021.09.003

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