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Recurrent and founder mutations in the Netherlands: Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutation.
Aalberts JJ, Schuurman AG, Pals G, Hamel BJ, Bosman G, Hilhorst-Hofstee Y, Barge-Schaapveld DQ, Mulder BJ, van den Berg MP, van Tintelen JP. Aalberts JJ, et al. Among authors: schuurman ag. Neth Heart J. 2010 Feb;18(2):85-9. doi: 10.1007/BF03091743. Neth Heart J. 2010. PMID: 20200614 Free PMC article.
16 results