LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections-Reference-Cited by-同舟云学术

LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections

Published:2016-03-18 Issue:6 Volume:118 Page:928-934
ISSN:0009-7330
Container-title:Circulation Research
language:en
Short-container-title:Circ Res

Author:

Guo Dong-chuan¹,Regalado Ellen S.¹,Gong Limin¹,Duan Xueyan¹,Santos-Cortez Regie Lyn P.¹,Arnaud Pauline¹,Ren Zhao¹,Cai Bo¹,Hostetler Ellen M.¹,Moran Rocio¹,Liang David¹,Estrera Anthony¹,Safi Hazim J.¹,Leal Suzanne M.¹,Bamshad Michael J.¹,Shendure Jay¹,Nickerson Deborah A.¹,Jondeau Guillaume¹,Boileau Catherine¹,Milewicz Dianna M.¹,

Affiliation:

1. From the Departments of Internal Medicine (D.G., E.S.R., L.G., X.D., Z.R., B.C., E.M.H., D.M.M.) and Cardiothoracic and Vascular Surgery (A.E., H.J.S.), University of Texas Health Science Center, Houston; Department of Molecular and Human Genetics, Center for Statistical Genetics, Baylor College of Medicine, Houston, TX (R.L.P.S.-C., S.M.L.); Laboratory for Vascular Translational Science, INSERM U1148, Hôpital Bichat, Paris, France (P.A., G.J., C.B.); Centre National de Référence pour le syndrome de...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference27 articles.

1. Familial thoracic aortic dilatations and dissections: A case control study

2. Familial Thoracic Aortic Aneurysms and Dissections—Incidence, Modes of Inheritance, and Phenotypic Patterns

3. Heterozygous TGFBR2 mutations in Marfan syndrome

4. Mutations in Transforming Growth Factor-β Receptor Type II Cause Familial Thoracic Aortic Aneurysms and Dissections

5. Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

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