טוען...
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...
שמור ב:
| הוצא לאור ב: | Genet Test Mol Biomarkers |
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| Main Authors: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Mary Ann Liebert, Inc.
2014
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| נושאים: | |
| גישה מקוונת: | 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 |
| תגים: |
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