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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Auteurs principaux:	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:	Artigo
Langue:	Inglês
Publié:	MDPI AG 2021-11-01
Collection:	Cells
Sujets:	<i>GDF2</i> hereditary hemorrhagic telangiectasia pulmonary arterial hypertension massive parallel sequencing NGS genomic medicine
Accès en ligne:	https://www.mdpi.com/2073-4409/10/11/3178
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