A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1

• Irene Johnsrud ,

  * E-mail: iejohnsrud@gmail.com

  Current address: Institute of Clinical Medicine, University of Oslo, N 0316, Oslo, Norway

  Affiliation Department of Dermatology, Oslo University Hospital, Rikshospitalet, N 0027, Oslo, Norway

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• Mari Ann Kulseth,

  Affiliation Department of Medical Genetics, Oslo University Hospital, N 0027, Oslo, Norway

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• Olaug Kristin Rødningen,

  Affiliation Department of Medical Genetics, Oslo University Hospital, N 0027, Oslo, Norway

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• Linn Landrø,

  Current address: Institute of Clinical Medicine, University of Oslo, N 0316, Oslo, Norway

  Affiliation Department of Dermatology, Oslo University Hospital, Rikshospitalet, N 0027, Oslo, Norway

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• Per Helsing,

  Affiliation Department of Dermatology, Oslo University Hospital, Rikshospitalet, N 0027, Oslo, Norway

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• Erik Waage Nielsen,

  Current address: Institute of Clinical Medicine, University of Oslo, N 0316, Oslo, Norway; Faculty of Health Sciences, University of Tromsø, 9037, Tromsø, Norway; Faculty of Professional Studies, University of Nordland, 8049, Bodø, Norway

  Affiliation Department of Anesthesiology, Nordland Hospital, N 8092, Bodø, Norway

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• Ketil Heimdal

  Affiliation Department of Medical Genetics, Oslo University Hospital, N 0027, Oslo, Norway

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