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Analysis of p.Gly12Valfs*2, p.Trp24* and p.Trp77Arg mutations in GJB2 and p.Arg81Gln variant in LRTOMT among non syndromic hearing loss Egyptian patients: implications for genetic diagnosis
Gibriel, Abdullah A., Abou-Elew, Maha H., Masmoudi, SaberLanguage:
english
Journal:
Molecular Biology Reports
DOI:
10.1007/s11033-019-04667-0
Date:
February, 2019
File:
PDF, 943 KB
english, 2019