A novel mutation in the glutaryl‐CoA dehydrogenase gene (GCDH) in an Iranian patient affected with Glutaric acidemia type 1

by Sima Rayat, Saeid Morovvati
Published 2021-09-01

Detecting Rare Triple Heteroplasmic Substitutions in the Mitochondrial DNA Control Region:A Potential Concern for Forensic DNA Studies

by Saeid Morovvati, Ziba Morovvati, Reza Ranjbar
Published 2011-01-01

A Study of Ribotype Patterns of Salmonella Enterica Serovar Enteritidis Strains Isolated in Tehran, Iran

by Reza Ranjbar, Meysam Sarshar, Saeid Morovvati
Published 2012-05-01

Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations

by Farzaneh Nasirnejad Sola, Saeid Morovvati, Mitra Sabetghadam Moghadam, Malihe Entezari
Published 2020-12-01

Mutation Analysis of ECM1 Gene in Two Related Iranian Patients Affected by Lipoid Proteinosis

by Saeid Morovvati, Paniz Farshadyeganeh, Mojdeh Hamidizadeh, Ziba Morovvati, Samaneh Doost Mohammadi
Published 2018-08-01

Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation

by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati
Published 2021-09-01

Hereditary Ataxia with a Novel Mutation in the Senataxin Gene: A Case Report

by Ehsan Moghanloo, Ziba Morovvati, Maghsoud Seifi, Fatemeh Minoochehr, Saeid Morovvati, Shahram Teimourian
Published 2019-05-01

A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia

by Marzieh Rahbaran, Maryam Hassani Doabsari, Simindokht Salavitabar, Neda Mokhberian, Ziba Morovvati, Saeid Morovvati
Published 2019-08-01

Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family

by Ziba Morovvati, Saeid Morovvati, Gholamhossein Alishiri, Seyed Hossein Moosavi, Reza Ranjbar, Yaser Bolouki Moghaddam
Published 2014-03-01

Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report

by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati
Published 2021-02-01