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A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients
Zhang, Z. P., Falk, G., Blomback, M., Egberg, N., Anveret, M.Volume:
1
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/1.9.767
Date:
December, 1992
File:
PDF, 311 KB
english, 1992