Persistent URL of this record https://hdl.handle.net/1887/98909
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The clinical spectrum of missense mutations of the first aspartic acid of cbEGF-like domains in fibrillin-1 including a recessive family
- All authors
- Hilhorst-Hofstee, Y.; Rijlaarsdam, M.E.B.; Scholte, A.J.H.A.; Swart-van den Berg, M.; Versteegh, M.I.M.; Schoot-van Velzen, I. van der; Schabitz, H.J.; Bijlsma, E.K.; Baars, M.J.; Kerstjens-Frederikse, W.S.; Giltay, J.C.; Hamel, B.C.; Breuning, M.H.; Pals, G.
- Date
- 2010
- Journal
- Human Mutation