مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

THE IRANIAN HUMAN MUTATION DATABASE

Pages

  372-375

Keywords

Not Registered.

Abstract

 Introduction ore than 20 years have elapsed since the first single base pair substitution underlying an inherited disease in humans was characterized at the DNA level. Disease-associated gene lesions are currently collected and publicized by the Human Gene Mutation Database (HGMD) in Cardiff, locusspecific mutation databases, and to some extent by the Genome Database (GDB) and Online Mendelian Inheritance in Man (OMIM) as comprehensive and up-to-date resources for information on genetic disorders and mutations causing them.1 – 4

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  • Cite

    APA: Copy

    MOTAZACKER, M.M., TAHERZADEH FARD, E., BEHJATI, F., ESTEGHAMAT, F.A.S., KAHRIZI, K., & NAJMABADI, H.. (2007). THE IRANIAN HUMAN MUTATION DATABASE. ARCHIVES OF IRANIAN MEDICINE, 10(3), 372-375. SID. https://sid.ir/paper/280230/en

    Vancouver: Copy

    MOTAZACKER M.M., TAHERZADEH FARD E., BEHJATI F., ESTEGHAMAT F.A.S., KAHRIZI K., NAJMABADI H.. THE IRANIAN HUMAN MUTATION DATABASE. ARCHIVES OF IRANIAN MEDICINE[Internet]. 2007;10(3):372-375. Available from: https://sid.ir/paper/280230/en

    IEEE: Copy

    M.M. MOTAZACKER, E. TAHERZADEH FARD, F. BEHJATI, F.A.S. ESTEGHAMAT, K. KAHRIZI, and H. NAJMABADI, “THE IRANIAN HUMAN MUTATION DATABASE,” ARCHIVES OF IRANIAN MEDICINE, vol. 10, no. 3, pp. 372–375, 2007, [Online]. Available: https://sid.ir/paper/280230/en

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