Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia

Author(s)

Journal

  • Thromb Haemost.

    Thromb Haemost. 104, 858-859, 2010

Cited by:  1

  • Transient hemiparesis in a 14-year-old boy with MYH9 disorders

    KITAMURA Katsumasa , KUNISHIMA Shinji , TAHARA Mayu , OGIWARA Shigetoshi , DOBATA Nana , DOBATA Tomoyuki , SUGIHARA Akemi , NAKASHIMA Taiji , SASAKI Yasushi , NAGUMO Kiyoshi , KUBOTA Mitsuru , KINUGAWA Yoshikazu , IEKO Masahiro , KUMAKI Satoru

    International journal of hematology 96(3), 376-379, 2012-09-01

    Ichushi Web  References (10)

Codes

  • NII Article ID (NAID)
    20000517357
  • Article Type
    Journal Article
  • Data Source
    CJPref 
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