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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
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 |
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