Congenital diaphragmatic abnormalities in arterial tortuosity syndrome patients who carry mutations in the SLC2A10 gene

Authors

  • SHE Zaidi,

    Corresponding author
    1. Division of Cardiology, Department of Medicine, University Health Network, Toronto, Ontario, Canada
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  • S Meyer,

    1. Universitaetsklinikum des Saarlandes, Kirrberger Strasse, Homburg, Germany
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  • I Peltekova,

    1. Department of Medicine, Queens University, Kingston, Ontario, Canada
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  • AS Teebi,

    1. Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar
    2. Department of Pediatrics, Weill Cornell Medical College, Doha, Qatar
    3. Section of Clinical Genetics and Dysmorphology, Hospital for Sick Children, Toronto, Ontario, Canada
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  • M Faiyaz-Ul-Haque

    1. Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
    2. Department of Genetics, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
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Syed HE Zaidi
Division of Cardiology
Department of Medicine
University Health Network
101 College Street
TMDT East Tower
Room 3-910
Toronto
Ontario M5G 1L7
Canada
Tel.: 416 581-7491
Fax: 1-416 581-7489
e-mail: syed.zaidi@uhnres.utoronto.ca

No abstract is available for this article.

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