Viewing StudyNCT00341874



Ignite Creation Date: 2024-05-05 @ 4:55 PM
Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00341874
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2024-06-10
First Post: 2006-06-19

Brief Title: Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan
Sponsor: National Institute on Deafness and Other Communication Disorders NIDCD
Organization: National Institutes of Health Clinical Center CC

Conditions & Keywords Data

Conditions:
Name
Hearing Disorder
Keywords:
Name View
Natural History View
DNA Mutations View
Genetic Variations View
GENETIC LINKAGE View
Usher Syndrome View
BLINDNESS View