Literature DB >> 20108392

Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive.

Fatemeh Alasti1, Nils Peeters, Wim Wuyts, Mohammad Hossein Sanati, Guy Van Camp.   

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Year:  2010        PMID： 20108392

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


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  1 in total

1.  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
  1 in total

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