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A Novel Nonsense Mutation (c.414G>A; p.Trp138*) in CLDN14 Causes Hearing Loss in Yemeni Families: A Case Report.
Mohamed, Walaa Kamal Eldin; Mahfood, Mona; Al Mutery, Abdullah; Abdallah, Sallam Hasan; Tlili, Abdelaziz.
Affiliation
  • Mohamed WKE; Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates.
  • Mahfood M; Departament de Genètica i de Microbiologia, Facultat de Biociències, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Al Mutery A; Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates.
  • Abdallah SH; Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates.
  • Tlili A; Human Genetics & Stem Cells Research Group, Research Institute of Sciences & Engineering, University of Sharjah, Sharjah, United Arab Emirates.
Front Genet ; 10: 1087, 2019.
Article in En | MEDLINE | ID: mdl-31781163
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Prognostic_studies Language: En Journal: Front Genet Year: 2019 Document type: Article Affiliation country: United Arab Emirates Country of publication: Switzerland
Fulltext
Add to My VHL
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Prognostic_studies Language: En Journal: Front Genet Year: 2019 Document type: Article Affiliation country: United Arab Emirates Country of publication: Switzerland