ΔC in Exon 18 of the von Willebrand Gene Is Uncommon in German vWD Type III Patients

• References

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• 4 Zhang ZP, Falk G, Blombäck M, Egberg N, Anvret M. A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients. Hum Mol Gen 1992; 1: 767-788
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