Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia
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ID: 270287
2018
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Abstract
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular disorder that leads to abnormal connections between arteries and veins termed arteriovenous malformations (AVM). Mutations in TGFβ pathway members ALK1, ENG and SMAD4 ...
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| Reference Key |
meadows2018angiogenesisvascular
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|---|---|
| Authors | Angela M. Crist, Amanda R. Lee, Nehal R. Patel, Dawn E. Westhoff, Stryder M. Meadows;Angela M. Crist;Amanda R. Lee;Nehal R. Patel;Dawn E. Westhoff;Stryder M. Meadows; |
| Journal | angiogenesis |
| Year | 2018 |
| DOI |
10.1007/s10456-018-9602-0
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| URL | |
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