Four novel genetic mutations are associated with patent foramen ovale in Tibetan population using whole exome sequencing

ObjectivePatent foramen ovale (PFO), a prevalent congenital cardiac defect, is linked to clinical conditions such as cryptogenic stroke and migraine. The genetic underpinnings of PFO remain poorly elucidated, particularly in Tibet. This study aimed to identify potential pathogenic mutations in Tibet...

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Bibliographic Details
Main Authors:	Hongwei Li, Yongjun He, Yong Wu, Lanxin Liu, Wei Du, Duika Wang, Zeng He, Liming Zhao
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2025-08-01
Series:	Frontiers in Genetics
Subjects:	pathogenetic mutations whole exome sequencing patent foramen ovale Tibetan genetics
Online Access:	https://www.frontiersin.org/articles/10.3389/fgene.2025.1592306/full
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Four novel genetic mutations are associated with patent foramen ovale in Tibetan population using whole exome sequencing

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