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NCT02575430

RET NAT 01

Natural History Study in Inherited Retinal Disease Subjects Caused by Mutations in RPE65 or LRAT.

Type: Observational



Status of the trial: Completed

Orphan Drug Recognition: NA

Inclusion

  • Opening Date: 2015-12-01
  • Closing Date: 2016-03-01

Criteria

More information

Children: Yes

Adults: Yes

Funder Type: industry

Principal location of the trial

HCP: Other investigators


Within ERN-EYE members

Workgroups

  • Retinal Rare Eye Diseases (WG1)

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