A missense mutation G109R in the PROC gene associated with type i protein C deficiency in a young Polish man with acute myocardial infarction

International Journal of Cardiology

Volumn 167, Issue 5, 2013, Pages

  Wypasek, Ewa ^a,b   Pankiw Bembenek, Oksana ^a,b   Potaczek, Daniel P ^a   Alhenc Gelas, Martine ^c   Trebacz, Jaroslaw ^a   Undas, Anetta ^a,b  

^a Krakowski Szpital Specjalistyczny Im Jana Pawła II   (Poland)

^b JAGIELLONIAN UNIVERSITY MEDICAL COLLEGE   (Poland)

^c HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

Author keywords

Mutation; PROC; Protein C deficiency; STEMI

Indexed keywords

ABCIXIMAB; ACETYLSALICYLIC ACID; C REACTIVE PROTEIN; CLOPIDOGREL; ENOXAPARIN; HEPARIN; PROTEIN KINASE C; TROPONIN I;

ACUTE HEART INFARCTION; ADULT; AKINESIA; ANGIOCARDIOGRAPHY; BODY TEMPERATURE MEASUREMENT; CASE REPORT; CLINICAL FEATURE; CONSERVATIVE TREATMENT; CORONARY ARTERY OBSTRUCTION; CORONARY ARTERY THROMBOSIS; DISEASE ASSOCIATION; ENZYME LINKED IMMUNOSORBENT ASSAY; FOLLOW UP; GENE; GENE FUNCTION; GENE IDENTIFICATION; GENETIC ASSOCIATION; HEART LEFT VENTRICLE EJECTION FRACTION; HUMAN; LETTER; LEUKOCYTOSIS; MALE; MEDICAL HISTORY; MISSENSE MUTATION; MOLECULAR DYNAMICS; MOLECULAR PATHOLOGY; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN KINASE C GENE; TRANSTHORACIC ECHOCARDIOGRAPHY;

MUTATION; PROC; PROTEIN C DEFICIENCY; STEMI;

ADULT; HUMANS; MALE; MUTATION, MISSENSE; MYOCARDIAL INFARCTION; PROTEIN C; PROTEIN C DEFICIENCY;

EID: 84883263094     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2013.04.102     Document Type: Article

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