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Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome.
Published in:
Science Translational Medicine, 2010, v. 2, n. 23, p. 1, doi. 10.1126/scitranslmed.3000488
By:
- Loeys, B. L.;
- Gerber, E. E.;
- Riegert-Johnson, D.;
- Iqbal, S.;
- Whiteman, P.;
- McConnell, V.;
- Chillakuri, C. R.;
- Macaya, D.;
- Coucke, P. J.;
- De Paepe, A.;
- Judge, D. P.;
- Wigley, F.;
- Davis, E. C.;
- Mardon, H. J.;
- Handford, P.;
- Keene, D. R.;
- Sakai, L. Y.;
- Dietz, H. C.
Publication type:
Article
Endothelial dysfunction and compromised eNOS/Akt signaling in the thoracic aorta during the progression of Marfan syndrome.
Published in:
2007
By:
- Chung, A W Y;
- Au Yeung, K;
- Cortes, S F;
- Sandor, G G S;
- Judge, D P;
- Dietz, H C;
- van Breemen, C
Publication type:
journal article