## 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
β¦ LIBER β¦
Molecular characterization of five Italian families with inherited severe factor XIII deficiency
β Scribed by G. CASTAMAN; S. H. GIACOMELLI; V. IVASKEVICIUS; V. SCHROEDER; H. P. KOHLER; A. DRAGANI; C. BIASIOLI; J. OLDENBURG; D. MADEO; F. RODEGHIERO
- Book ID
- 108772916
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 304 KB
- Volume
- 0
- Category
- Article
- ISSN
- 1351-8216
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