7 results on '"Sedghi, Maryam"'
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2. Understanding the impact of DIS3 cancer-associated mutations by in silico structure modeling
3. D5S351 and D5S1414 located at the spinal muscular atrophy critical region represent novel informative markers in the Iranian population
4. Structural and functional impact of missense mutations in TPMT: An integrated computational approach
5. Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation
6. Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries
7. Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1
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