Expanding the Evidence of a Semi-Dominant Inheritance in GDF2 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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Detalles Bibliográficos
Autores principales: Gallego, Natalia, Cruz-Utrilla, Alejandro, Guillén, Inmaculada, Bonora, Amparo Moya, Ochoa, Nuria, Arias, Pedro, Lapunzina, Pablo, Escribano-Subias, Pilar, Nevado, Julián, Tenorio-Castaño, Jair
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8624726/
https://www.ncbi.nlm.nih.gov/pubmed/34831401
http://dx.doi.org/10.3390/cells10113178

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8624726/
https://www.ncbi.nlm.nih.gov/pubmed/34831401
http://dx.doi.org/10.3390/cells10113178

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