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Identification of the CFTR p.Phe508Del founder mutation in the absence of a polythymidine 9T allele in a Hispanic patient

Authors

  • N Dharajiya,

    1. Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA
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    • Current address: Department of Pathology, University of California San Diego, San Diego, La Jolla, CA, USA

    • These authors contributed equally to this work.

  • KM Chisholm,

    1. Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA
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    • These authors contributed equally to this work.

  • L Dietz,

    1. Molecular Pathology Laboratory, Stanford Hospital and Clinics, Stanford, CA, USA
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  • C Sue Richards,

    1. Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, USA
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  • M Kharrazi,

    1. Genetic Disease Screening Program, California Department of Public Health, Richmond, CA, USA
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  • I Schrijver

    Corresponding author
    1. Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA
    • Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA
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Correspondence:

Iris Schrijver, MD

Department of Pathology, L235

Stanford University, School of Medicine

300 Pasteur Drive

Stanford, CA 94305, USA

Tel.: 650-724-2403

Fax: 650-724-1567

e-mail: ischrijver@stanfordmed.org

No abstract is available for this article.

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