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Paper Details

Identification of rare sequence variation underlying heritable pulmonary arterial hypertension.
Nat Commun
242
2018
AQP1, ATP13A3, BMPR2, BMPR2 ligand, GDF2, PAH, PAH genes, Pulmonary arterial hypertension, SOX17, bone morphogenetic protein type 2 receptor, heritable pulmonary arterial hypertension, putative, rare sequence variation, transfected cells
Author NameAffiliation
Stefan Gr??fUniversity of Cambridge
Stefan Gr??fUniversity of Cambridge
Stefan Gr??f
Matthias HaimelUniversity of Cambridge
Matthias HaimelUniversity of Cambridge
Matthias Haimel
Marta BledaUniversity of Cambridge
Louise C DaughertyUniversity of Cambridge
Louise C Daugherty
Louise C DaughertyUniversity of Cambridge
Louise C Daugherty
Inga ProkopenkoImperial College London
Florent SoubrierAssistance Publique-Hopitaux de Paris, INSERM, UPMC Sorbonne Universites
Emilia M SwietlikUniversity of Cambridge
Willem H OuwehandUniversity of Cambridge
Willem H Ouwehand
Willem H OuwehandUniversity of Cambridge
Willem H Ouwehand
Nicole SoranzoUniversity of Cambridge
Nicole SoranzoWellcome Trust Sanger Institute
Nicole SoranzoUniversity of Cambridge
Nicole SoranzoWellcome Trust Sanger Institute
Richard C TrembathKing's College London
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