Genotyping Data and Novel Haplotype Diversity of STR Markers in the SLC26A4 Gene Region in Five Ethnic Groups of the Iranian Population

Background and Aims: SLC26A4 gene mutations are the second currently identifiable genetic cause of autosomal recessive nonsyndromic hearing loss after GJB2 mutations. Because of the extensive size of the SLC26A4 gene and the variety of mutations, indirect diagnosis using linkage analysis has been su...

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Bibliographische Detailangaben
Veröffentlicht in:Genet Test Mol Biomarkers
Hauptverfasser: Mojtabavi Naeini, Marjan, Mesrian Tanha, Hamzeh, Hashemzadeh Chaleshtori, Morteza, Vallian, Sadeq
Format: Artigo
Sprache:Inglês
Veröffentlicht: Mary Ann Liebert, Inc. 2014
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Original Articles
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4250946/
https://ncbi.nlm.nih.gov/pubmed/25390158
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2014.0178
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