3613948
Last Update Posted: 2021-10-25
Recruiting has ended
All Genders accepted | 4 months-75 Years |
280 Estimated Participants | No Expanded Access |
Observational Study | Does not accept healthy volunteers |
Study on the Effects of Mutations Under Inherited Retinal Disease in Korean
To develop comprehensive genetic maps of inherited retinal diseases in Korean
- Establishment of comprehensive genetic database in Koreans with inherited retinal diseases including frequently mutated genes, genotype-phenotype correlations, and visual prognosis."
Group/ Cohort Label : Subject with age between 6 months and 65 years who have not receive molecular genetic testing Group / Cohort Description : Consecutive subjects with inherited retinal disease who are willing to do genetic testing using whole exome sequencing (n=265) and whole genome sequencing (n=15) and agree to informed consent of the study
Eligibility
Relevant conditions:
Inherited Retinal Dystrophy Primarily Involving Sensory Retina
Inherited Retinal Dystrophy Primarily Involving Retinal Pigment Epithelium
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the trial if you think are close to fitting criteria.
locations
Contact Information
Overall Contact
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Data sourced from ClinicalTrials.gov