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Volumn 13, Issue 9, 2015, Pages 1735-1736
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Challenges in implementation of ISTH diagnostic algorithm for diagnosis and classification of factor XIII deficiency in Iran
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Author keywords
[No Author keywords available]
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Indexed keywords
BLOOD CLOTTING FACTOR 8;
AUTOANTIBODY;
BLOOD CLOTTING FACTOR 13;
PROTEIN SUBUNIT;
BLOOD CLOTTING FACTOR 13 DEFICIENCY;
CLASSIFICATION ALGORITHM;
CONSANGUINEOUS MARRIAGE;
DIAGNOSTIC TEST;
FAMILY HISTORY;
FXIII GENE;
GENE;
GENE MUTATION;
HUMAN;
IMMUNOASSAY;
IRAN;
LABORATORY TEST;
LETTER;
MOLECULAR DIAGNOSIS;
MUTATIONAL ANALYSIS;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
ALGORITHM;
BLOOD;
BLOOD CLOTTING;
BLOOD CLOTTING TEST;
BLOOD EXAMINATION;
CHEMISTRY;
CLASSIFICATION;
CONSANGUINITY;
ECONOMICS;
EXON;
FACTOR XIII DEFICIENCY;
GENETICS;
IMMUNOLOGY;
INCIDENCE;
MISSENSE MUTATION;
POINT MUTATION;
PROCEDURES;
PROTEIN SUBUNIT;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
SOLUBILITY;
THROMBOCYTE;
ALGORITHMS;
AUTOANTIBODIES;
BLOOD COAGULATION;
BLOOD COAGULATION TESTS;
BLOOD PLATELETS;
CONSANGUINITY;
EXONS;
FACTOR XIII;
FACTOR XIII DEFICIENCY;
HEMATOLOGIC TESTS;
HUMANS;
INCIDENCE;
IRAN;
MUTATION, MISSENSE;
POINT MUTATION;
POLYMERASE CHAIN REACTION;
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
PROTEIN SUBUNITS;
SOLUBILITY;
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EID: 84940893087
PISSN: 15387933
EISSN: 15387836
Source Type: Journal
DOI: 10.1111/jth.13037 Document Type: Letter |
Times cited : (22)
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References (5)
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