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NCT00422721

Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy

Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy.

Type: Interventional



Status of the trial: Completed

Orphan Drug Recognition: NA

Inclusion

  • Opening Date: 2007-04-01
  • Closing Date: 2011-11-24

Criteria

More information

Children: Yes

Adults: Yes

Funder Type: public

Principal location of the trial

HCP: Principal investigators


Within ERN-EYE members

Workgroups

  • Retinal Rare Eye Diseases (WG1)

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This ERN is supported by: