Phenotype-genotype characterization of 1
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Flora Peyvandi; Liliana Tagliabue; Marzia Menegatti; Mehran Karimi; Istvan KomΓ‘r
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Article
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2003
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John Wiley and Sons
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English
β 149 KB
## 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