CLINICAL_TRIALS
research
· 2013-10-14
Clinical Trial Update: Clinical and Molecular Characterisation of Orofaciodigital Syndromes and Other Clinical Phenotypes Secondary to Mutations in the OFD1 Gene
Summary
Clinical trial update focusing on clinical and molecular characterization of Orofaciodigital syndromes and other phenotypes caused by OFD1 mutations.
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Diseases / indications
Snippet
Sponsor: Centre Hospitalier Universitaire Dijon | Conditions: Orofaciodigital Syndromes | Status: UNKNOWN