分子病態部
研究業績
  1. Nagaya S, Maruyama K, Watanabe A, Meguro-Horike M, Imai Y, Hiroshima Y, Horike SI, Kokame K, Morishita E. First report of inherited protein S deficiency caused by paternal PROS1 mosaicism. Haematologica. 107, 330-333, 2022.