Mutations in fibrillin-1 cause congenital scleroderma: Stiff skin syndrome

B. L. Loeys, E. E. Gerber, D. Riegert-Johnson, S. Iqbal, P. Whiteman, V. McConnell, C. R. Chillakuri, D. Macaya, P. J. Coucke, A. De Paepe, D. P. Judge, F. Wigley, E. C. Davis, H. J. Mardon, P. Handford, D. R. Keene, L. Y. Sakai, H. C. Dietz

Research output: Contribution to journalArticle

Fingerprint Dive into the research topics of 'Mutations in fibrillin-1 cause congenital scleroderma: Stiff skin syndrome'. Together they form a unique fingerprint.

Medicine & Life Sciences