Molecular mechanism for hereditary protein C deficiency in two Chinese families with thrombosis

Journal of Thrombosis and Haemostasis

Volumn 4, Issue 5, 2006, Pages 1154-1156

  Zhou, R F ^a,b   Cai, X H ^a   Xie, S ^a   Wang, X F ^a   Wang, Hong Li ^a  

^a SHANGHAI SECOND MEDICAL UNIVERSITY   (China)

^b NANJING UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN C;

ARTICLE; CELL STRAIN COS7; CHINESE; CLINICAL FEATURE; DEEP VEIN THROMBOSIS; DISEASE ASSOCIATION; DISEASE SEVERITY; DNA SEQUENCE; EXON; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENETIC DISORDER; GENOTYPE; HETEROZYGOSITY; HIGH RISK PATIENT; HUMAN; IMMUNOHISTOCHEMISTRY; MESENTERIC VEIN THROMBOSIS; MISSENSE MUTATION; MOLECULAR MECHANICS; NONHUMAN; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN ANALYSIS; PROTEIN C DEFICIENCY; PROTEIN DEGRADATION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN SECRETION; RECURRENT DISEASE; RISK ASSESSMENT; SEQUENCE ANALYSIS; VEIN THROMBOSIS; WILD TYPE;

ADULT; CHINA; FEMALE; HETEROZYGOTE; HUMANS; MALE; MUTATION, MISSENSE; PEDIGREE; PROTEIN C DEFICIENCY; THROMBOSIS;

EID: 33645647884     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2006.01913.x     Document Type: Article

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