A single cytosine deletion in exon 18 of the von Willebrand...

Human Molecular Genetics 1992 / 12 Vol. 1; Iss. 9

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.
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
1
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/1.9.767
Date:
December, 1992
File:
PDF, 311 KB
english, 1992
Conversion to is in progress
Conversion to is failed