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Browsing by Author Genderen, M. van

Full Text	Issue Date	Title	Author(s)
	2009	A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa	Azam, M.; Khan, M.I.; Gal, A.; Hussain, A.; Shah, S.T., et al
	2009	A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.	Littink, K.W.; Genderen, M. van; Collin, R.W.J.; Roosing, S.; Brouwer, A.P.M. de, et al
	2009	Genotyping microarray for CSNB-associated genes.	Zeitz, C.; Labs, S.; Lorenz, B.; Forster, U.; Uksti, J., et al
	2005	Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.	Zeitz, C.; Genderen, M. van; Neidhardt, J.; Luhmann, U.F.; Hoeben, F., et al