Long Non-Coding RNA Expression Profiles in Hereditary Haemorrhagic Telangiectasia

Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominantly inherited vascular disease characterized by the presence of mucocutaneous telangiectasia and arteriovenous malformations in visceral organs. HHT is predominantly caused by mutations in ENG and ACVRL1, which both belong to the TG...

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Detalles Bibliográficos
Autores principales: Tørring, Pernille M., Larsen, Martin Jakob, Kjeldsen, Anette D., Ousager, Lilian Bomme, Tan, Qihua, Brusgaard, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946172/
https://www.ncbi.nlm.nih.gov/pubmed/24603890
http://dx.doi.org/10.1371/journal.pone.0090272

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946172/
https://www.ncbi.nlm.nih.gov/pubmed/24603890
http://dx.doi.org/10.1371/journal.pone.0090272

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