𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

✍ Scribed by Johnson, D.W.; Berg, J.N.; Baldwin, M.A.; Gallione, C.J.; Marondel, I.; Yoon, S.-J.; Stenzel, T.T.; Speer, M.; Pericak-Vance, M.A.; Diamond, A.


Book ID
109916279
Publisher
Nature Publishing Group
Year
1996
Tongue
English
Weight
896 KB
Volume
13
Category
Article
ISSN
1061-4036

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Novel missense and frameshift mutations
✍ Daniel J. Klaus; Carol J. Gallione; Kara Anthony; Eric Y. Yeh; Jing Yu; Andreas 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 47 KB 👁 3 views

Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disorder characterized by multisystemic vascular dysplasia and recurrent hemorrhage. One of the causative genes is the activin receptor-like kinase-1 (ALK-1) gene located on chromosome 12q13. ALK-1 is an endothelial cell type I rec