Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency.
about
Historical perspective and future direction of coagulation research.Hereditary protein C deficiency in Indian patients with venous thrombosis.Hereditary Thrombophilic Disease Associated with Defects in the Protein C Anticoagulant System.The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X.High prevalence of congenital thrombophilia in patients with pregnancy-related or idiopathic venous thromboembolism/pulmonary embolism.Cellular processing of the amyloidogenic cystatin C variant of hereditary cerebral hemorrhage with amyloidosis, Icelandic type
P2860
Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Impaired secretion of the elon ...... reditary protein C deficiency.
@en
type
label
Impaired secretion of the elon ...... reditary protein C deficiency.
@en
prefLabel
Impaired secretion of the elon ...... reditary protein C deficiency.
@en
P2093
P2860
P356
P1476
Impaired secretion of the elon ...... reditary protein C deficiency.
@en
P2093
P2860
P304
P356
10.1172/JCI116135
P407
P577
1992-12-01T00:00:00Z