Marzieh Mojbafan

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 8

Top Topics

End Stage Renal Disease

Genome Wide Identification

Top Venues

Clinical case reports

Molecular genetics & genomic medicine

Nucleosides, nucleotides & nucleic acids

This page only lists publications with an associated author ORCID identifier.

Publications

Saeed Ghasemi, Marzieh Mojbafan, Saeed Talebi, Nakysa Hooman, Rozita Hoseini
Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population. Molecular genetics & genomic medicine 12 (4) (2024)
Saeed Ghasemi, Marzieh Mojbafan, Saeed Talebi, Nakysa Hooman, Rozita Hoseini
Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population. Molecular genetics & genomic medicine 12 (4) (2024)
Maryam Kachuei, Kiana Orangi, Aynaz Mohammadi, Mohammad Mohammadi, Marzieh Mojbafan
Bethlem myopathy: A novel homozygous variant of c.385C>T (p.Arg129Cys) in the COL6A2 gene. Clinical case reports 12 (8) (2024)
Shima Salehi, Amir Hozhabrpour, Somayeh Takrim Nojehdeh, Marzieh Mojbafan
Association between polymorphism at codon 469 of the ICAM-1 gene and Henoch-Schönlein purpura in an Iranian cohort. Nucleosides, nucleotides & nucleic acids (2024)
Maryam Kachuei, Kiana Orangi, Aynaz Mohammadi, Mohammad Mohammadi, Marzieh Mojbafan
Bethlem myopathy: A novel homozygous variant of c.385C>T (p.Arg129Cys) in the COL6A2 gene. Clinical case reports 12 (8) (2024)
Saeed Ghasemi, Marzieh Mojbafan, Saeed Talebi, Nakysa Hooman, Rozita Hoseini
Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population. Molecular genetics & genomic medicine 12 (4) (2024)
Somayeh Takrim Nojehdeh, Marzieh Mojbafan, Nakysa Hooman, Rozita Hoseini, Hasan Otukesh
Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation. Clinical case reports 10 (12) (2022)
Somayeh Takrim Nojehdeh, Marzieh Mojbafan, Nakysa Hooman, Rozita Hoseini, Hasan Otukesh
Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation. Clinical case reports 10 (12) (2022)