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

No abstract is available for this paper.

• Publication year

  2019

• Venue

  Molecular Biology Reports

• Publication date

  2019-02-07

• Fields of study

  Medicine

• Identifiers
  DOI 10.1007/s11033-019-04667-0PMID 30730013
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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