Your browser does not support JavaScript or JavaScript is not enabled. Without JavaScript some functions of this webapplication may be disabled or cause error messages. To enable JavaScript, please consult the manual of your browser or contact your system administrator.

Project

Exploring the role of non-coding variation in inherited retinal dystrophies: NMNAT1 regulatory mutations as a proof of concept

Information

Project Team

Organisations

Outputs and Outcomes

Promotor

Elfride De Baere

Department of Pediatrics and medical genetics

Copromotor

Frauke Coppieters

Department of Pediatrics and medical genetics