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A novel mutation in PRDM5 in brittle cornea syndrome

Authors

  • MA Aldahmesh,

    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
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  • JY Mohamed,

    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
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  • FS Alkuraya

    Corresponding author
    1. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
    2. Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia
    3. Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
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Fowzan S. Alkuraya, MD
Developmental Genetics Unit
Department of Genetics
King Faisal Specialist Hospital and Research Center
MBC-03
PO BOX 3354
Riyad 11211
Saudi Arabia
Tel: +966 1 442 7875
Fax: +966 1 442 4585
e-mail: falkuraya@kfshrc.edu.sa

No abstract is available for this article.

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