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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2011
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3194820/
https://ncbi.nlm.nih.gov/pubmed/22022569
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0026206
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