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Clinical trial

Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing

NCT02558478 is registered in ClinicalTrials.gov with University Hospital, Strasbourg, France as lead sponsor.

NCT NCT02558478
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Registry record

As filed in ClinicalTrials.gov.

Title
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing
Lead sponsor
University Hospital, Strasbourg, France
Phase
Observational
Overall status
Unknown status
Start date
September 30, 2015
Completion date
September 30, 2018
Enrollment
39 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

hearing loss, neurosensory diseases, retinopathy