Get access

A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite patients in North America

Authors

  • Catrina Loucks,

    1. Department of Medical Genetics, Alberta Children's Hospital and Alberta Children's Hospital Research Institute for Child and Maternal Health, University of Calgary, Calgary, Alberta, Canada
    Search for more papers by this author
  • Jillian S. Parboosingh,

    1. Department of Medical Genetics, Alberta Children's Hospital and Alberta Children's Hospital Research Institute for Child and Maternal Health, University of Calgary, Calgary, Alberta, Canada
    Search for more papers by this author
  • Jessica X. Chong,

    1. Department of Human Genetics, The University of Chicago, Chicago, Illinois
    Search for more papers by this author
  • Carole Ober,

    1. Department of Human Genetics, The University of Chicago, Chicago, Illinois
    2. Department of Obstetrics and Gynecology, The University of Chicago, Chicago, Illinois
    Search for more papers by this author
  • Victoria M. Siu,

    1. Department of Paediatrics and Biochemistry, University of Western Ontario, London, Ontario, Canada
    Search for more papers by this author
  • Robert A. Hegele,

    1. Departments of Biochemistry and Medicine, Robarts Research Institute and Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada
    Search for more papers by this author
  • C. Anthony Rupar,

    1. Department of Paediatrics and Biochemistry, University of Western Ontario, London, Ontario, Canada
    Search for more papers by this author
  • D. Ross McLeod,

    1. Department of Medical Genetics, Alberta Children's Hospital and Alberta Children's Hospital Research Institute for Child and Maternal Health, University of Calgary, Calgary, Alberta, Canada
    Search for more papers by this author
  • Alfredo Pinto,

    1. Department of Pathology and Lab Medicine, University of Calgary, Calgary, Alberta, Canada
    Search for more papers by this author
  • Albert E. Chudley,

    1. Program in Genetic and Metabolism, Children's Hospital, Department of Pediatrics and Child Health and Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada
    Search for more papers by this author
  • A. Micheil Innes

    Corresponding author
    1. Department of Medical Genetics, Alberta Children's Hospital and Alberta Children's Hospital Research Institute for Child and Maternal Health, University of Calgary, Calgary, Alberta, Canada
    • Department of Medical Genetics, 2888 Shaganappi Trail NW, Calgary, Canada AB T3B 6A8.

    Search for more papers by this author

  • How to Cite this Article: Loucks C, Parboosingh JS, Chong JX, Ober C, Siu VM, Hegele RA, Rupar CA, McLeod DR, Pinto A, Chudley AE, Innes AM. 2012. A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite patients in North America. Am J Med Genet Part A. 158A:1229–1232.

Ancillary