Keywords = Mutation
Number of Articles: 9
1. Analysis of KRAS gene mutation associated with Helicobacter pylori infection in patients with gastric cancer

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

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


2. 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

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


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

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

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


4. 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

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


5. Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family

Volume 19, Issue 7, July 2016, Pages 772-778

Somayeh Reiisi; Mohammad Amin Tabatabaiefar; Mohammad Hosein Sanati; Morteza Hashemzadeh Chaleshtori


6. Diagnosis of genetic defects through parallel assessment of PLCĪ¶ and CAPZA3 in infertile men with history of failed oocyte activation

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

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


7. 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

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


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

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

Fatemeh Khatami; Mohammad Mehdi Heidari; Massoud Houshmand


9. Novel Missense Mitochondrial ND4L Gene Mutations in Friedreich's Ataxia

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

Mohammad Mehdi Heidari; Mehri Khatami