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Molecular Medicine Reports
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Print ISSN: 1791-2997 Online ISSN: 1791-3004
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March-April 2011 Volume 4 Issue 2

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International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

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International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

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Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

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Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

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Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

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Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

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International Journal of Functional Nutrition

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Article

Mutations of the Connexin 26 gene in families with non-syndromic hearing loss

  • Authors:
    • Walid Al-Achkar
    • Faten Moassass
    • Bassel Al-Halabi
    • Ayman Al-Ablog
  • View Affiliations / Copyright

    Affiliations: Department of Molecular Biology and Biotechnology, Division of Human Genetics, Atomic Energy Commission, Damascus, Syria
  • Pages: 331-335
    |
    Published online on: January 25, 2011
       https://doi.org/10.3892/mmr.2011.428
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Abstract

Autosomal recessive non-syndromic hearing impairment (ARNSHI) is caused by mutations in the gap junction gene GJB2 (Connexin 26; Cx26) in numerous human populations. The aim of this study was to determine the frequency of six GJB2 mutations in 50 Syrian families with congenital deafness and in 180 controls. PCR-RFLP was used to detect the 35delG, 167delT, M34T, W24X, W77R and E47X mutations, and direct sequencing was performed for the 35delG mutation. The data revealed a high prevalence of the 35delG mutation among deaf families. Homozygous 35delG was detected in fifteen of the Syrian families (30%). A compound heterozygous genotype was observed in two families: one with the 35delG/167delT mutation (2%) and one with the 35delG/M34T mutation (2%). Nine families were heterozygous with no second identified mutation in Cx26: four with 35delG+/unknown (8%), four with 167delT/unknown (8%) and one with M34T/unknown (2%). The W24X, W77R and E47X mutations were not detected in any of the study subjects. Three individuals with the heterozygous 35delG genotype (1.66%) and five with the heterozygous 167delT genotype (2.77%) were detected among the controls. No other mutations were found among the controls. These results have important implications for the diagnosis and counseling of families with Cx26 deafness.

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Copy and paste a formatted citation
Spandidos Publications style
Al-Achkar W, Moassass F, Al-Halabi B and Al-Ablog A: Mutations of the Connexin 26 gene in families with non-syndromic hearing loss. Mol Med Rep 4: 331-335, 2011.
APA
Al-Achkar, W., Moassass, F., Al-Halabi, B., & Al-Ablog, A. (2011). Mutations of the Connexin 26 gene in families with non-syndromic hearing loss. Molecular Medicine Reports, 4, 331-335. https://doi.org/10.3892/mmr.2011.428
MLA
Al-Achkar, W., Moassass, F., Al-Halabi, B., Al-Ablog, A."Mutations of the Connexin 26 gene in families with non-syndromic hearing loss". Molecular Medicine Reports 4.2 (2011): 331-335.
Chicago
Al-Achkar, W., Moassass, F., Al-Halabi, B., Al-Ablog, A."Mutations of the Connexin 26 gene in families with non-syndromic hearing loss". Molecular Medicine Reports 4, no. 2 (2011): 331-335. https://doi.org/10.3892/mmr.2011.428
Copy and paste a formatted citation
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Spandidos Publications style
Al-Achkar W, Moassass F, Al-Halabi B and Al-Ablog A: Mutations of the Connexin 26 gene in families with non-syndromic hearing loss. Mol Med Rep 4: 331-335, 2011.
APA
Al-Achkar, W., Moassass, F., Al-Halabi, B., & Al-Ablog, A. (2011). Mutations of the Connexin 26 gene in families with non-syndromic hearing loss. Molecular Medicine Reports, 4, 331-335. https://doi.org/10.3892/mmr.2011.428
MLA
Al-Achkar, W., Moassass, F., Al-Halabi, B., Al-Ablog, A."Mutations of the Connexin 26 gene in families with non-syndromic hearing loss". Molecular Medicine Reports 4.2 (2011): 331-335.
Chicago
Al-Achkar, W., Moassass, F., Al-Halabi, B., Al-Ablog, A."Mutations of the Connexin 26 gene in families with non-syndromic hearing loss". Molecular Medicine Reports 4, no. 2 (2011): 331-335. https://doi.org/10.3892/mmr.2011.428
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