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A familial factor XIII subunit B deficiency

โœ Scribed by Masanori Saito; Hidesaku Asakura; Tomotaka Yoshida; Keiko Ito; Kazuhiro Okafuji; Takashi Yoshida; Tamotsu Matsuda


Book ID
114711976
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
406 KB
Volume
74
Category
Article
ISSN
0007-1048

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FACTOR XIII SUBUNIT B DEFICIENCY
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Phenotype-genotype characterization of 1
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## Communicated by Edward Tuddenham Factor XIII (FXIII) deficiency is a very rare severe autosomal bleeding disorder with a frequency of 1:2,000,000 in the general population and only a few patients have been genetically characterized so far. We report a phenotype-genotype characterization of 10 u