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
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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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