Genetic Study of Patients With Primary Ciliary Dyskinesia
NCT00005650 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 180
Last updated 2005-06-24
Summary
OBJECTIVES:
I. Characterize the clinical presentation of patients with primary ciliary dyskinesia.
II. Identify the genetic mutations associated with this disease.
Conditions
- Primary Ciliary Dyskinesia
Sponsors & Collaborators
-
University of North Carolina
collaborator OTHER -
National Center for Research Resources (NCRR)
lead NIH
Principal Investigators
-
Peadar G. Noone · University of North Carolina
Eligibility
- Min Age
- 0 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2000-02-29
Countries
- United States
Study Locations
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