Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran

Autor: Hosseinipour, A., Chaleshtori, M. H., Sasanfar, R., Farhud, D. D., Tolooi, A., Doulati, M., Rad, L. H., Mostafa Montazer zohour, Ghadami, M.

Publikováno v: Iranian Journal of Public Health, Vol 34, Iss 1, Pp 47-50 (2005)
Scopus-Elsevier
Iranian Journal of Public Health, Vol 34, Iss 1 (2005)

Autosomal recessive and sporadic non-syndromic hearing loss (ARSNSHL) is the major form of hereditary deafness.Mutations in the GJB2 gene encoding the gap-junction protein Connexin 26 have been identified to be highly associated with ARSNSHL. In this

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http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/908.pdf&manuscript_id=908