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Significant liver disease in a patient with Y116H mutation in the MVK gene

Authors

  • Melissa Leyva-Vega,

    1. Division of Gastroenterology, Hepatology and Nutrition, University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, 19104
    Current affiliation:
    1. Division of Gastroenterology and Nutrition, Department of Pediatrics, Hackensack University School of Medicine, Hackensack, New Jersey 07601.
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  • Pamela F. Weiss,

    1. Division of Rheumatology, University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, 19104
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  • Jaya Ganesh,

    1. Division of Human Genetics, Department of Pediatrics, University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, 19104
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  • Laura Conlin,

    1. Department of Pathology, University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, 19104
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  • Nancy B. Spinner,

    1. Department of Pathology, University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, 19104
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  • Randolph P. Matthews

    Corresponding author
    1. Division of Gastroenterology, Hepatology and Nutrition, University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, 19104
    • Division of Gastroenterology, Hepatology and Nutrition, University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
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  • How to Cite this Article: Leyva-Vega M, Weiss PF, Ganesh J, Conlin L, Spinner NB, Matthews RP. 2011. Significant liver disease in a patient with Y116H mutation in the MVK gene. Am J Med Genet Part A 155:1461–1464.

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