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Information Journal Paper

Title

HIGH FREQUENCY OF 35DELG MUTATION IN GJB2 ASSOCIATED WITH AUTOSOMAL RECESSIVE NONSYNDROMIC HEARING LOSS (ARNSHL) IN THE PROVINCE OF ISFAHAN-IRAN

Pages

  2074-2078

Abstract

 Several reports from different regions of Iran indicate the importance of 35delG mutation in GJB2 gene. In the present study, mutation frequency of 35delG in the population of Autosomal Recessive Non-Syndromic HEARING LOSS (ARNSHL) was investigated in the province of ISFAHAN. Sixty-three ISFAHANi unrelated patients with ARNSHL were included in the study. Patients were screened for the 35delG mutation in GJB2 using allele refraction mutation system/PCR (ARMS/PCR) followed by sequencing. Of 126 studied chromosomes, 39 (31.0%) were found to be positive for 35delG mutation. Because 35delG mutation shows a relatively high frequency in most parts of Iran, the population of ISFAHAN could be considered as populations with a high frequency of the mutation.

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  • Cite

    APA: Copy

    REZAEI, HALIMEH, VALLIAN BROOJENI, SADEQ, & MOVAHEDI, REZVAN. (2010). HIGH FREQUENCY OF 35DELG MUTATION IN GJB2 ASSOCIATED WITH AUTOSOMAL RECESSIVE NONSYNDROMIC HEARING LOSS (ARNSHL) IN THE PROVINCE OF ISFAHAN-IRAN. GENETICS IN THE 3RD MILLENNIUM, 8(3), 2074-2078. SID. https://sid.ir/paper/117225/en

    Vancouver: Copy

    REZAEI HALIMEH, VALLIAN BROOJENI SADEQ, MOVAHEDI REZVAN. HIGH FREQUENCY OF 35DELG MUTATION IN GJB2 ASSOCIATED WITH AUTOSOMAL RECESSIVE NONSYNDROMIC HEARING LOSS (ARNSHL) IN THE PROVINCE OF ISFAHAN-IRAN. GENETICS IN THE 3RD MILLENNIUM[Internet]. 2010;8(3):2074-2078. Available from: https://sid.ir/paper/117225/en

    IEEE: Copy

    HALIMEH REZAEI, SADEQ VALLIAN BROOJENI, and REZVAN MOVAHEDI, “HIGH FREQUENCY OF 35DELG MUTATION IN GJB2 ASSOCIATED WITH AUTOSOMAL RECESSIVE NONSYNDROMIC HEARING LOSS (ARNSHL) IN THE PROVINCE OF ISFAHAN-IRAN,” GENETICS IN THE 3RD MILLENNIUM, vol. 8, no. 3, pp. 2074–2078, 2010, [Online]. Available: https://sid.ir/paper/117225/en

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