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Non-Syndromic autosomal recessive deafness in Gaza strip: A study of five GJB2 Gene mutations

Essammak, Badria F; Ashour, Mohammed J.; Sharif, Fadel A. (2014)
Hearing loss is a common, pan-ethnic and highly heterogeneous sensory disorder with an incidence of around 1 in 1000 infants. Genetic causes are thought to be responsible for more than 60% of the cases with the majority ...

The institutional repository of the Islamic University of Gaza was established as part of the ROMOR project that has been co-funded with support from the European Commission under the ERASMUS + European programme. This publication reflects the views only of the author, and the Commission cannot be held responsible for any use which may be made of the information contained therein.

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Author
Ashour, Mohammed J. (1)
Essammak, Badria F (1)
Sharif, Fadel A. (1)
Subjectarnshl (1)
cx26 (1)
gaza strip (1)
gjb2 (1)
mutation (1)
pcr-rflp (1)
... View MoreDate Issued2014 (1)

The institutional repository of the Islamic University of Gaza was established as part of the ROMOR project that has been co-funded with support from the European Commission under the ERASMUS + European programme. This publication reflects the views only of the author, and the Commission cannot be held responsible for any use which may be made of the information contained therein.

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