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RSFVEN-330/2010
Retinitis pigmentosa: molecular diagnosis by next generation sequencing
Retinitis pigmentosa: molecular diagnosis by next generation sequencing.
Type: Observational
Status of the trial: Completed
Orphan Drug Recognition: No
Inclusion
- Opening Date: 2013-06-18
- Closing Date: 2016-09-19
Criteria
Inclusion: probands or family pedigrees with inherited retinal dystrophy
Exclusion: patients or family pedigrees with retinal abnormalities mimiking inherited retinal dystrophy
Children: No
Adults: Yes
Funder Type: public
HCP: Principal investigators
HCP: Other investigators
Within ERN-EYE members
Workgroups
Retinal Rare Eye Diseases (WG1)