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Fine mapping of the hereditary haemorrhagic telangiectasia (HHT)3 locus on chromosome 5 excludes VE-Cadherin-2, Sprouty4 and other interval genes
BACKGROUND: There is significant interest in new loci for the inherited condition hereditary haemorrhagic telangiectasia (HHT) because the known disease genes encode proteins involved in vascular transforming growth factor (TGF)-β signalling pathways, and the disease phenotype appears to be unmasked...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2010
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2924844/ https://ncbi.nlm.nih.gov/pubmed/20701797 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2384-2-15 |
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