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A Genetic Analysis of Usher Syndrome in Ashkenazi Jews
This study has been completed.
Study NCT00016471   Information provided by National Center for Research Resources (NCRR)
First Received: May 7, 2001   Last Updated: June 23, 2005   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Usher Syndrome
Retinitis Pigmentosa
Congenital Hearing Impairment
Additional conditions recognized in this trial
Deafness
Hearing Loss
Retinitis
Retrocochlear Diseases
Syndrome
Usher Syndromes
More general conditions related to this trial
Abnormalities, Multiple
Blindness
Congenital Abnormalities
Deaf-Blind Disorders
Disease
Ear Diseases
Eye Diseases
Eye Diseases, Hereditary
Genetic Diseases, Inborn
Hearing Disorders
Hearing Loss, Sensorineural
Nervous System Diseases
Neurologic Manifestations
Otorhinolaryngologic Diseases
Pathologic Processes
Retinal Degeneration
Retinal Diseases
Sensation Disorders
Signs and Symptoms
Vision Disorders
Interventions listed in this trial
Audiogram
Electroretinogram
Sponsors listed in this trial
National Center for Research Resources (NCRR)


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