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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...
Autores principales: | Tørring, Pernille M., Larsen, Martin Jakob, Kjeldsen, Anette D., Ousager, Lilian Bomme, Tan, Qihua, Brusgaard, Klaus |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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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 |
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