Projects per year
Search results
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Active
Functional Characterization of biallelic mutations of Centrobin as causative of Seckel-like syndrome
1/1/24 → 12/31/25
Project: Internal Grants (IG)
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Finished
Characterization of Hitherto Undiagnosed Adult Neurogenetic Disorders in Oman
9/1/19 → 8/31/21
Project: MoHERI
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Functional characterization of RYR3 mutations associated with neurodevelopment disorders.
1/1/19 → 12/31/20
Project: Internal Grants (IG)
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Identifying Genetic causes of Autosomal Recessive Intellectual Disability
1/1/16 → 12/31/20
Project: Consultancy project
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A new paradigm for the molecular diagnosis of uncharacterized genetic disorders in the Omani population
9/1/14 → 5/31/18
Project: MoHERI
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The genetics of cardiometabolic disorders among Arabs of Oman Family Study
9/1/14 → 8/31/17
Project: MoHERI
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Molecular epidemiology and diagnosis study of common inborn errors of metabolism disorders in Oman and UAE: Phase 2
1/1/14 → 12/31/14
Project: Other project