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

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

Research output: Contribution to journal/periodicalArticleScientificpeer-review

Original languageEnglish
Pages (from-to)730-736
JournalAmerican Journal of Human Genetics
Volume85
DOIs
Publication statusPublished - 2009

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