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

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

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