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Mononuclear cells and vascular repair in HHT

Hereditary hemorrhagic telangiectasia (HHT) or Rendu–Osler–Weber disease is a rare genetic vascular disorder known for its endothelial dysplasia causing arteriovenous malformations and severe bleedings. HHT-1 and HHT-2 are the most prevalent variants and are caused by heterozygous mutations in endog...

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Detalles Bibliográficos
Autores principales:	Dingenouts, Calinda K. E., Goumans, Marie-José, Bakker, Wineke
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2015
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369645/ https://www.ncbi.nlm.nih.gov/pubmed/25852751 http://dx.doi.org/10.3389/fgene.2015.00114

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