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

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Title:	Recurrent and founder mutations in the Netherlands. Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutations.
Author(s):	Aalberts, J.J.J. Schuurman, A.G. Pals, G. (152870326) Hamel, B.C.J. (079063632) Bosman, G.J.C.G.M. (069365431) Hilhorst-Hofstee, Y. Barge-Schaapveld, D.Q.C.M. Mulder, B.J.M. Berg, M.P. van den Tintelen, J.P. van
Publication year:	2010
Document type:	Article / Letter to editor
Journal:	Netherlands Heart Journal
ISSN:	1568-5888
Volume:	vol. 18
Issue:	iss. 2
Start page:	p. 85
End page:	p. 89
Subject:	DCN 2: Functional Neurogenomics IGMD 3: Genomic disorders and inherited multi-system disorders
Organization:	UMCN Extern Human Genetics Biochemistry (UMCN)
Appears in Collections:	Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/89447