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

Research group Kamermans
Publication year 2009
Published in American Journal of Human Genetics
Authors M.M. Van Genderen, I. Fahrenfort, Y.B. Claassen, R.J. Florijn, J.N. Pearring, F. Meire, M.A. McCall, F.C.C. Riemslag, R.G. Gregg, A.A.B. Bergen, M. Kamermans
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