Recurrent and founder mutations in the Netherlands: Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutation

J.J.J. Aalberts, A.G. Schuurman, G. Pals, B.J.C. Hamel, G. Bosman, Y. Hilhorst-Hofstee, D.Q.C.M. Barge-Schaapveld, B.J.M. Mulder, M.P. van den Berg, J. van Tintelen

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

Original languageEnglish
Title of host publicationFounder mutations in inherited cardiac diseases in the Netherlands
Publication statusPublished - 2014

Cite this