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Prospective study of visual function in USHER syndrome induced by MYO7A mutation and retinotosis pigmentosa.
Status of the trial: Unknown
Orphan Drug Recognition: NA
- Opening Date: 2017-11-03
- Closing Date: 2019-11-04
Inclusion: USH1B group: genotype with two pathogenic mutations of the MYO7A gene RP group: a genotype with a pathogenic mutation identified. For all: Diagnosis of confirmed retinopathy pigmentosa
Exclusion: Persons who have previously participated in a clinical trial of gene therapy or with ocular disease or ocular opacity. History of amblyopia
Funder Type: industry, public
HCP: Principal investigators
HCP: Other investigators
Within ERN-EYE members
- Retinal Rare Eye Diseases (WG1)
This ERN is supported by: