A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33–34
✍ Scribed by McDonald, M.T.; Papenberg, K.A.; Ghosh, S.; Glatfelter, A.A.; Biesecker, B.B.; Helmbold, E.A.; Markel, D.S.; Zolotor, A.; McKinnon, W.C.; Vanderstoep, J.L.
- Book ID
- 109915150
- Publisher
- Nature Publishing Group
- Year
- 1994
- Tongue
- English
- Weight
- 582 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1061-4036
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## Abstract Hereditary hemorrhagic telangiectasia (HHT) is a genetically and clinically heterogeneous multisystem vascular dysplasia. Mutations of the endoglin and __ACVRL1__ genes are known to cause HHT. However, existence of HHT families in which linkage to these genes has been excluded has sugge