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DIIO_EPPR_P13_03

Retinitis pigmentosa: molecular diagnosis by next generation sequencing

Retinitis pigmentosa: molecular diagnosis by next generation sequencing.

Type: Observational



Status of the trial: Active, Not recruiting

Orphan Drug Recognition: NA

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: Yes

Adults: Yes

Funder Type: patient organisation

Principal location of the trial

HCP: Principal investigators


Within ERN-EYE members

Principal investigators




Other investigators

Workgroups

  • Retinal Rare Eye Diseases (WG1)

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This ERN is supported by: