Morteza Oladnabi
14PUBLICATIONS
6CO-AUTHORS
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Publications (14)
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|Dec 31, 2025
Molecular dynamics insights into novel and nano-rare de novo mutations in the ribosomal proteins S19 and L26 causing Diamond-Blackfan anemia in Iranian patients.Teymoor Khosravi, Mohaddese Mohsenipour, Hanieh Mohtashamiasl
|Dec 23, 2025
A novel Bi-Allelic pathogenic MCOLN1 variant underlying mucolipidosis type IV in an Iranian family: clinical, genetic, and molecular dynamics-based structural analysis.Mohaddese Mohsenipour, Parham Nejati, Teymoor Khosravi
|Dec 17, 2025
A case study of a novel homozygous EDAR splice site variant in hypohidrotic ectodermal dysplasia with tooth agenesis: molecular dynamics insights.Parham Nejati, Teymoor Khosravi, Saba Lorestani
|Nov 04, 2025
A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.Parham Nejati, Nafiseh Falsafi, Elham Alimoradi
|Nov 29, 2024
A novel frameshift variant in the TMPRSS3 gene causes nonsyndromic hearing loss in a consanguineous family.Nahid Rezaie, Saeedeh Sadat Ghazanfari, Seyede Mahsa Mousavikia
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