Expanding the Evidence of a Semi-Dominant Inheritance in <i>GDF2</i> Associated with Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) sometimes co-exists with hereditary hemorrhagic telangiectasia (HHT). Despite being clinically diagnosable according to Curaçao criteria, HHT can be difficult to diagnose due to its clinically heterogenicity and highly overlapping with PAH. Genetic analysis of t...

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Bibliographic Details

Published in:	Cells
Main Authors:	Natalia Gallego, Alejandro Cruz-Utrilla, Inmaculada Guillén, Amparo Moya Bonora, Nuria Ochoa, Pedro Arias, Pablo Lapunzina, Pilar Escribano-Subias, Julián Nevado, Jair Tenorio-Castaño
Format:	Article
Language:	English
Published:	MDPI AG 2021-11-01
Subjects:	<i>GDF2</i> hereditary hemorrhagic telangiectasia pulmonary arterial hypertension massive parallel sequencing NGS genomic medicine
Online Access:	https://www.mdpi.com/2073-4409/10/11/3178