Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474.
- Cited forVARIANT THPH5 CYS-515, CHARACTERIZATION OF VARIANT PROS1 DEFICIENCY CYS-515, MUTAGENESIS OF ARG-515
- CategoriesSequences, Disease & Variants
- SourceUniProtKB reviewed (Swiss-Prot)
- PubMed
- Europe PMC
- Blood 87:4643-4650 ()
Cited in