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A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy
Brouwer, A.P.M. de; Nabuurs, S.B.; Verhaart, I.E.C.; Oudakker, A.R.; Hordijk, R.; Yntema, H.G.; ... ; Kleefstra, T. 2014
A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy
Article / Letter to editor
metadata only
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
Ven, J.P.H. van de; Nilsson, S.C.; Tan, P.L.; Buitendijk, G.; Ristau, T.; Mohlin, F.C.; ... ; Hollander, A.I. den 2013
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
Article / Letter to editor
metadata only
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
Ven, J.P.H. van de; Nilsson, S.C.; Tan, P.L.; Buitendijk, G.H.S.; Ristau, T.; Mohlin, F.C.; ... ; Hollander, A.I. den 2013
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
Article / Letter to editor
metadata only
Solution structure of the second PDZ domain of the neuronal adaptor X11alpha and its interaction with the C-terminal peptide of the human copper chaperone for superoxide dismutase
Duquesne, A.E.; Ruijter, M. de; Brouwer, J.; Drijfhout, J.W.; Nabuurs, S.B.; Spronk, C.A.E.M.; ... ; Canters, G.W. 2005
Solution structure of the second PDZ domain of the neuronal adaptor X11alpha and its interaction with the C-terminal peptide of the human copper chaperone for superoxide dismutase
Article / Letter to editor
open access
2006-01-02T00:00:00Z