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Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Author:

Maria M. van Genderen,Mieke M.C. Bijveld,Yvonne B. Claassen,Ralph J. Florijn,Jillian N. Pearring,Francoise M. Meire,Maureen A. McCall,Frans C.C. Riemslag,Ronald G. Gregg,Arthur A.B. Bergen,Maarten Kamermans

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

13 November 2009

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