Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression system.

Source:http://linkedlifedata.com/resource/pubmed/id/9531593

Blood 1998 Apr 15 91 8 2830-8

Download in:

View as

Triples

General Info

PMID
9531593