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Retinitis pigmentosa: molecular diagnosis by next generation sequencing.
Status of the trial: Active, Not recruiting
Orphan Drug Recognition: NA
Inclusion: probands or family pedigrees with inherited retinal dystrophy
Exclusion: patients or family pedigrees with retinal abnormalities mimiking inherited retinal dystrophy
Funder Type: patient organisation
Principal location of the trial
HCP: Principal investigators
HCP: Other investigators