Keywords = Mutation
Number of Articles: 10
The worldwide frequency of MYO15A gene mutations in patients with autosomal recessive non-syndromic hearing loss: A meta‐analysis

Volume 23, Issue 7, July 2020, Pages 841-848

10.22038/ijbms.2020.35977.8563

Mahsa Farjami; Reza Asadi; Fahimeh Afzal Javan; Malihe Alimardani; Saeed Eslami; Sima Mansoori Derakhshan; Atieh Eslahi; Majid Mojarad

Analysis of KRAS gene mutation associated with Helicobacter pylori infection in patients with gastric cancer

Volume 22, Issue 5, May 2019, Pages 529-533

10.22038/ijbms.2019.32047.7707

Raheleh Jabini; Seyed Ahmad Eghbali; Hosein Ayatolahi; Maryam Sheikhi; Mohammadreza Farzanehfar

The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families

Volume 21, Issue 3, March 2018, Pages 333-341

10.22038/ijbms.2018.26269.6441

Ehsan Razmara; Fatemeh Bitarafan; Elika Esmaeilzadeh-Gharehdaghi; Navid Almadani; Masoud Garshasbi

Mutation analysis of connexin 50 gene among Iranian families with autosomal dominant cataracts

Volume 20, Issue 3, March 2017, Pages 288-293

10.22038/ijbms.2017.8358

Masoumeh Mohebi; Saeed Chenari; Abolfazl Akbari; Fariba Ghassemi; Mehran Zarei-Ghanavati; Ghasem Fakhraie; Nahid Babaie; Mansour Heidari

A novel deletion and two recurrent substitutions on type VII collagen gene in seven Iranian patients with epidermolysis bullosa

Volume 19, Issue 8, August 2016, Pages 858-862

10.22038/ijbms.2016.7467

Armita Kakavand Hamidi; Mohammad Moghaddam; Nasim Hatamnejadian; Ahmad Ebrahimi

Diagnosis of genetic defects through parallel assessment of PLCζ and CAPZA3 in infertile men with history of failed oocyte activation

Volume 19, Issue 3, March 2016, Pages 281-289

10.22038/ijbms.2016.6647

Soudabeh Javadian-Elyaderani; Kamran Ghaedi; Marziyeh Tavalaee; Farzaneh Rabiee; Mohammad Reza Deemeh; Mohammad Hossein Nasr-Esfahani

Mutation analysis of the phenylalanine hydroxylase gene in Azerbaijani population, a report from West Azerbaijan province of Iran

Volume 18, Issue 7, July 2015, Pages 649-653

10.22038/ijbms.2015.4645

Morteza Bagheri; Isa Abdi Rad; Nima Hosseini Jazani; Rasoul Zarrin; Ahad Ghazavi

The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family

Volume 17, Issue 9, September 2014, Pages 656-661

10.22038/ijbms.2014.3327

Fatemeh Khatami; Mohammad Mehdi Heidari; Massoud Houshmand

Novel Missense Mitochondrial ND4L Gene Mutations in Friedreich's Ataxia

Volume 14, Issue 3, May 2011, Pages 219-224

10.22038/ijbms.2011.4993

Mohammad Mehdi Heidari; Mehri Khatami

Iranian Journal of Basic Medical Sciences

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