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2015-17: Inherited Retinal Disease Clinical Study Protocol RET NAT 01

Children and inhertable diseases
Outcome research
Investigator Initiated Research
Inclusion open since 1-1-2016

Retrospective, Uncontrolled, Multicenter, Case History Study to Determine the Natural History of Visual Function in Subjects With Inherited Retinal Disease Caused by Inherited Mutation of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT).

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