Title : A patient with type 2N von Willebrand disease is heterozygous for a new mutation: Gly22Glu. Demonstration of a defective expression of the second allele by the use of monoclonal antibodies.

Pub. Date : 1997 May 1

PMID : 9129031






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Recombinant vWF (rvWF) containing the candidate mutation was transiently expressed in COS-7 cells. carbonyl sulfide von Willebrand factor Homo sapiens