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Endoplasmic Reticulum Quality Control Is Involved in the Mechanism of Endoglin-Mediated Hereditary Haemorrhagic Telangiectasia

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition affecting the vascular system and is characterised by epistaxis, arteriovenous malformations and mucocutaneous and gastrointestinal telangiectases. This disorder affects approximately 1 in 8,000 people worldwide....

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Detalles Bibliográficos
Autores principales:	Ali, Bassam R., Ben-Rebeh, Imen, John, Anne, Akawi, Nadia A., Milhem, Reham M., Al-Shehhi, Nouf A., Al-Ameri, Mouza M., Al-Shamisi, Shamma A., Al-Gazali, Lihadh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2011
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194820/ https://www.ncbi.nlm.nih.gov/pubmed/22022569 http://dx.doi.org/10.1371/journal.pone.0026206

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