SMAD4 gene mutation increases the risk of aortic dilation in patients with hereditary haemorrhagic telangiectasia-Reference-Cited by-同舟云学术

SMAD4 gene mutation increases the risk of aortic dilation in patients with hereditary haemorrhagic telangiectasia

Published:2017-10 Issue: Volume:245 Page:114-118
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Vorselaars V.M.M.,Diederik A.,Prabhudesai V.,Velthuis S.,Vos J.-A.,Snijder R.J.,Westermann C.J.J.,Mulder B.J.,Ploos van Amstel J.K.,Mager J.J.,Faughnan M.E.,Post M.C.

Funder

Nelson Arthur Hyland Foundation

Li Ka Shing Knowledge Institute

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference33 articles.

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3. Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1;McAllister;Nat. Genet.,1994

4. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4);Gallione;Lancet,2004

5. Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review;Wain;Genet. Med.,2014

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