Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290

Authors

  • S.R. Ghaffari,

    Corresponding author
    1. Comprehensive Genetic Center, Hope Generation Foundation, Tehran, Iran
    2. Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran
    3. Gene Clinic, Tehran, Iran
    • Correspondence:

      Dr Saeed Reza Ghaffari, MSc, MD, PhD

      21, Shabahang Building

      26, Dr Gharib Street

      Keshavarz Blvd

      1419783517 Tehran

      Iran

      Tel.: +98 21 66935655

      Fax: +98 21 66933336

      e-mail: saeed@ghaffari.org

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  • M. Rafati,

    1. Comprehensive Genetic Center, Hope Generation Foundation, Tehran, Iran
    2. Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran
    3. Gene Clinic, Tehran, Iran
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  • G. Ghaffari,

    1. Macdonald Department of Human Genetics, John P. Hussman Institute for Human Genomics and the Dr. John T Miller School of Medicine, University of Miami, Miami, FL, USA
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  • M. Morra,

    1. Macdonald Department of Human Genetics, John P. Hussman Institute for Human Genomics and the Dr. John T Miller School of Medicine, University of Miami, Miami, FL, USA
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  • M. Tekin

    1. Macdonald Department of Human Genetics, John P. Hussman Institute for Human Genomics and the Dr. John T Miller School of Medicine, University of Miami, Miami, FL, USA
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No abstract is available for this article.

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