Thromb Haemost 2015; 114(04): 862-863
DOI: 10.1160/TH15-01-0007
Letters to the Editor
Schattauer GmbH

Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations

Authors

  • Toshiyuki Miyata

    1   Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan
  • Yumiko Uchida

    1   Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan
  • Toshiyuki Ohta

    2   Department of Pediatric Nephrology, Hiroshima Prefectural Hospital, Hiroshima, Japan
  • Kohtaro Urayama

    2   Department of Pediatric Nephrology, Hiroshima Prefectural Hospital, Hiroshima, Japan
  • Yoko Yoshida

    3   Department of Blood Transfusion Medicine, Nara Medical University, Kashihara, Japan
  • Yoshihiro Fujimura

    3   Department of Blood Transfusion Medicine, Nara Medical University, Kashihara, Japan

Financial support: This work was supported in part by grants-in-aid from the Ministry of Health, Labour and Welfare of Japan, the Japan Society for the Promotion of Science, and the Takeda Science Foundation.
Further Information

Publication History

Received: 06 January 2015

Accepted after major revision: 23 April 2015

Publication Date:
29 November 2017 (online)

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