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Clinical exome sequencing identified a nonsense mutation in TMC1 gene causing profound hearing loss / by Maryam Alobathani ; supervised by Abdullah Al Mutery, Abdelaziz Tlili.

By: Contributor(s): Material type: TextTextPublication details: 2019.Description: 40 leaves : col. ill. ; 30 cm.+ 1 CD-Rom (4 3/4 in.)Subject(s): NLM classification:
  • WV270
Online resources: Dissertation note: Thesis (M.Sc.)--University of Sharjah, 2019.
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