Marziyeh Mojbafan

6PUBLICATIONS
21CO-AUTHORS
Developmental genetics (incl. sex determination)Infant and child healthCell physiologyNutrigenomics and personalised nutritionNeonatology
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Publications (6)

|Jun 30, 2026
A Novel MYO5A Mutation (c.3508C>T) in a 27-Month-Old Girl With Hypotonia and Developmental Delay: Expanding the Phenotypic Spectrum of Griscelli Syndrome Type 1.

|Jun 03, 2026
Genetically Confirmed Hyperoxaluria in Iranian Children- A Multicenter Survey.

|Aug 13, 2024
Bethlem myopathy: A novel homozygous variant of c.385C>T (p.Arg129Cys) in the COL6A2 gene.

Maryam Kachuei, Kiana Orangi, Aynaz Mohammadi

|Apr 27, 2024
Association between polymorphism at codon 469 of the ICAM-1 gene and Henoch-Schönlein purpura in an Iranian cohort.

Shima Salehi, Amir Hozhabrpour, Somayeh Takrim Nojehdeh

|Apr 16, 2024
Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population.

Saeed Ghasemi, Marzieh Mojbafan, Saeed Talebi

|Dec 14, 2022
Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation.

Somayeh Takrim Nojehdeh, Marzieh Mojbafan, Nakysa Hooman

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Frequent Collaborators

2 joint publications

Nakysa Hooman

1 joint publications

Somayeh Takrim Nojehdeh

1 joint publications

Rozita Hoseini

1 joint publications

Hasan Otukesh