A novel mutation (Gln433Glu) in exon 12 combined with the G insertion in exon 13 causes severe factor XI deficiency in Japanese patients
- Nobutsune Ishikawa
- , Satoshi Okada
- , Takashi Sato
- , Shin'ichiro Yasunaga
- , Motoaki Ohtsubo
- , Yoshihiro Takihara
- , Masao Kobayashi
Research output: Contribution to journal › Article › peer-review
5
Scopus
citations