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Volumn 109, Issue 6, 2013, Pages 1180-1182
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Hypodysfibrinogenaemia and thrombosis in association with a new fibrinogen y chain with two mutations (γ114Tyr→His, and γ320Asp deleted)
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Author keywords
[No Author keywords available]
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Indexed keywords
FIBRINOGEN;
CASE REPORT;
CONTROLLED STUDY;
DISEASE ASSOCIATION;
DYSFIBRINOGENEMIA;
ELECTROSPRAY;
FIBRINOGEN BLOOD LEVEL;
GENE MUTATION;
HUMAN;
HYPODYSFIBRINOGENAEMIA;
LETTER;
LUNG EMBOLISM;
MALE;
NEWBORN;
POLYACRYLAMIDE GEL ELECTROPHORESIS;
PRIORITY JOURNAL;
PROTEIN ANALYSIS;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
THROMBIN TIME;
THROMBOSIS;
AFIBRINOGENEMIA;
ASPARTIC ACID;
BINDING SITES;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
DIMERIZATION;
FIBRINOGEN;
GENE DELETION;
GENETIC VARIATION;
HISTIDINE;
HUMANS;
INFANT;
MALE;
MUTATION;
PHENOTYPE;
SEQUENCE ANALYSIS, DNA;
THROMBOSIS;
TYROSINE;
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EID: 84878630969
PISSN: 03406245
EISSN: None
Source Type: Journal
DOI: 10.1160/TH13-01-0068 Document Type: Letter |
Times cited : (9)
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References (8)
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