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Association of the 3467C>T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's disease

✍ Scribed by P. Casaña; F. Martínez; S. Haya; C. Espinós; J. Aznar

Publisher: Springer
Year: 2001
Tongue: English
Weight: 46 KB
Volume: 80
Category: Article
ISSN: 0939-5555
DOI: 10.1007/s002770100307

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