Literature DB >> 21488234

Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndrome.

Mohammad Amin Tabatabaiefar1, Fatemeh Alasti, Nils Peeters, Wim Wuyts, Mohammad Reza Nooridaloii, Morteza Hashemzadeh Chaleshtori, Guy Van Camp.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2010        PMID： 21488234

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


× No keyword cloud information.
  2 in total

1.  Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian population.

Authors:  Marjan Mojtabavi Naeini; Hamzeh Mesrian Tanha; Morteza Hashemzadeh Chaleshtori; Sadeq Vallian
Journal:  Genet Test Mol Biomarkers       Date:  2014-12

2.  Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome.

Authors:  Nasrin Yazdanpanahi; Mohammad Amin Tabatabaiefar; Effat Farrokhi; Narges Abdian; Nader Bagheri; Shirin Shahbazi; Zahra Noormohammadi; Morteza Hashemzadeh Chaleshtori
Journal:  Clin Exp Otorhinolaryngol       Date:  2013-11-29       Impact factor: 3.372
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.