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

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

Principal investigators

Other investigators

Workgroups