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Identification of two novel missense mutations causing severe factor XIII deficiency.
- Published in:
- Haemophilia, 2015, v. 21, n. 3, p. e253, doi. 10.1111/hae.12663
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- Article
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.
- Published in:
- Haemophilia, 2014, v. 20, n. 4, p. 568, doi. 10.1111/hae.12340
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- Publication type:
- Article