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Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families

Authors

  • M Faiyaz-Ul-Haque,

    1. Program in Genetics and Genomic Biology, Hospital for Sick Children, Toronto, Ontario, Canada
    2. Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
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    • *

      These authors contributed equally to this work.

  • SHE Zaidi,

    1. Department of Medicine, University Health Network, Toronto, Ontario, Canada
    2. Department of Lung Biology, University of Toronto, Toronto, Ontario, Canada
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    • *

      These authors contributed equally to this work.

  • AA Wahab,

    1. Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar
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    • *

      These authors contributed equally to this work.

  • A Eltohami,

    1. Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar
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  • MS Al-Mureikhi,

    1. Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar
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  • G Al-Thani,

    1. Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar
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  • VD Peltekova,

    1. Hospital for Sick Children, Toronto, Ontario, Canada
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  • L-C Tsui,

    1. Program in Genetics and Genomic Biology, Hospital for Sick Children, Toronto, Ontario, Canada
    2. The University of Hong Kong, Hong Kong, China
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  • AS Teebi

    1. Program in Genetics and Genomic Biology, Hospital for Sick Children, Toronto, Ontario, Canada
    2. Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar
    3. Section of Clinical Genetics and Dysmorphology, Hospital for Sick Children, Toronto, Ontario, Canada
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Muhammad Faiyaz-Ul-Haque, MPhil, PhD
Molecular Genetics Laboratory
Department of Pathology and Laboratory Medicine
King Faisal Specialist Hospital and Research Centre
PO Box 3354
MBC 10
Riyadh 11211
Saudi Arabia
Tel.: 96614647272x 39637
Fax: 96614424280
e-mail: mfhaque@kfshrc.edu.sa

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