Functional Alterations Involved in Increased Bleeding in Hereditary Hemorrhagic Telangiectasia Mouse Models

Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal-dominant genetic disorder involving defects in two predominant genes known as endoglin (ENG; HHT-1) and activin receptor-like kinase 1 (ACVRL1/ALK1; HHT-2). It is characterized by mucocutaneous telangiectases that, due to their fragility, f...

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Detalles Bibliográficos
Autores principales: Egido-Turrión, Cristina, Rossi, Elisa, Ollauri-Ibáñez, Claudia, Pérez-García, María L., Sevilla, María A., Bastida, José María, González-Porras, José Ramón, Rodríguez-Barbero, Alicia, Bernabeu, Carmelo, Lopez-Novoa, José M., Pericacho, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160577/
https://www.ncbi.nlm.nih.gov/pubmed/35665360
http://dx.doi.org/10.3389/fmed.2022.871903

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160577/
https://www.ncbi.nlm.nih.gov/pubmed/35665360
http://dx.doi.org/10.3389/fmed.2022.871903

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