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A distinct common p.Gln317* mutation among causative LMAN1 genetic mutations of combined factor V and factor VIII deficiency in five Taiwanese families.

Hsuan-Yu LinJen-Shiou LinWoei TsayPo-Te LinYing-Chih HuangMing-Ching Shen
Published in: Haemophilia : the official journal of the World Federation of Hemophilia (2021)
Keyphrases
  • genome wide
  • replacement therapy