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

173 Citations (Scopus)
Original languageEnglish
Pages (from-to)730-736
JournalAmerican Journal of Human Genetics
Publication statusPublished - 2009

Cite this