Landscape of mutational profiles in a Polish cohort of patients diagnosed with idiopathic pulmonary arterial hypertension

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dc.contributor.authorBorys, Agnieszka M.
dc.contributor.authorJonas, Kamil
dc.contributor.authorSochacka, Ewelina
dc.contributor.authorKołton-Wróż, Maria
dc.contributor.authorWołkow, Paweł
dc.contributor.authorWypasek, Ewa
dc.contributor.authorPelc, Ewa
dc.contributor.authorMałecki, Maciej T.
dc.contributor.authorKopeć, Grzegorz
dc.contributor.authorTotoń-Żurańska, Justyna
dc.date.accessioned2026-06-24T07:41:23Z
dc.date.available2026-06-24T07:41:23Z
dc.date.issued2025-09-23
dc.description.abstractIntroduction: "Pulmonary arterial hypertension (PAH) is a rare vascular disorder, characterized by narrowing of the pulmonary arteries due to vasoconstriction and vascular remodeling [1–3]. The national registry reports a PAH incidence of 5.2 cases per million per year and a prevalence of 30.8 cases per million in Poland [4, 5]. While its etiology remains partly unclear, genetic factors have been implicated in certain patient groups [6–8]. However, the molecular background of this population has not been systematically studied. Therefore, we aimed to comprehensively characterize the genetic landscape of PAH in Polish patients." (...)
dc.identifier.citationKardiologia Polska. Polish Heart Journal 2026, Vol. 84, No 2
dc.identifier.doi10.33963/v.phj.108670
dc.identifier.eissn1897-4279
dc.identifier.issn0022-9032
dc.identifier.urihttps://hdl.handle.net/11315/31602
dc.language.isoen
dc.publisherVia Medica
dc.rightsCreative Commons Attribution International (CC BY) license
dc.subjectidiopathic pulmonary arterial hypertension
dc.subjectmutational profiles
dc.subject.otherMedycyna
dc.subject.otherZdrowie
dc.titleLandscape of mutational profiles in a Polish cohort of patients diagnosed with idiopathic pulmonary arterial hypertension
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