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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 journal › Article › peer-review
152
Scopus
citations