Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing
NCT02558478
·
clinicaltrials.gov ↗
UNKNOWN
Status
39
Enrollment
OTHER
Sponsor class
Conditions
Neurosensory Diseases
Retinopathy
Hearing Loss
Interventions
GENETIC:
blood sampling
Sponsor
University Hospital, Strasbourg, France