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Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.

Van Genderen, M.M. and Fahrenfort, I. and Claassen, Y.B. and Florijn, R.J. and Pearring, J.N. and Meire, F. and McCall, M.A. and Riemslag, F.C.C. and Gregg, R.G. and Bergen, A.A.B. and Kamermans, M. (2009) Mutations in TRPM1 are a common cause of complete congenital stationary night blindness. American Journal of Human Genetics, 85, 730-736. ISSN 0002-9297.

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Item Type:Article
Institutes:Netherlands Institute for Neuroscience (NIN)
ID Code:6714
Deposited On:18 Jan 2010 01:00
Last Modified:03 Aug 2010 14:32

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