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Browsing by Author Lee, K.

Full Text	Issue Date	Title	Author(s)
	2010	Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.	Schraders, M.; Lee, K.; Oostrik, J.; Huygen, P.L.M.; Ali, G., et al
	2009	TRPV5 gene polymorphisms in renal hypercalciuria.	Renkema, K.Y.; Lee, K.; Topala, C.N.; Goossens, M.; Houillier, P., et al
	2009	Parathyroid hormone activates TRPV5 via PKA-dependent phosphorylation.	Groot, T. de; Lee, K.; Langeslag, M.; Xi, Q.; Jalink, K., et al
	2008	Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.	Collin, R.W.J.; Kalay, E.; Tariq, M.; Peters, T.A.; Zwaag, B. van der, et al