Viewing StudyNCT00001871



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Last Modification Date: 2024-10-26 @ 9:02 AM
Study NCT ID: NCT00001871
Status: COMPLETED
Last Update Posted: 2008-03-04
First Post: 1999-11-03

Brief Title: Study of Muscle Abnormalities in Patients With Specific Genetic Mutations
Sponsor: National Heart Lung and Blood Institute NHLBI
Organization: National Institutes of Health Clinical Center CC

Conditions & Keywords Data

Conditions:
Name
Muscular Dystrophy Oculopharyngeal
Cardiomyopathy Hypertrophic
Keywords:
Name View
Genetic Mutations View
Hypertrophic Cardiomyopathy View
Oculopharyngeal Muscular Dystrophy View