Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran

Clinical and Applied Thrombosis/Hemostasis

Volumn 18, Issue 1, 2012, Pages 100-103

  Eshghi, Peyman ^a   Cohan, Nader ^b   Lak, Manigeh ^c   Naderi, Majid ^d   Peyvandi, Flora ^e   Menegatti, Marzia ^e   Karimi, Mehran ^b  

^a SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d ZAHEDAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^e UNIVERSITY OF MILAN   (Italy)

Author keywords

FXIII deficiency; Iran; Mutation

Indexed keywords

ARGININE; BLOOD CLOTTING FACTOR 13; HISTIDINE; TRYPTOPHAN;

AMINO ACID SUBSTITUTION; ARTICLE; BLOOD CLOTTING FACTOR 13 DEFICIENCY; CLINICAL ARTICLE; CONSANGUINEOUS MARRIAGE; DIAGNOSTIC TEST; DISEASE SEVERITY; FAMILY; FEMALE; GENETIC ANALYSIS; HIGH RISK PATIENT; HISTOPATHOLOGY; HUMAN; INHERITANCE; IRAN; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; RISK FACTOR; SCREENING TEST; SINGLE NUCLEOTIDE POLYMORPHISM;

AMINO ACID SUBSTITUTION; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; FACTOR XIII; FACTOR XIII DEFICIENCY; FEMALE; GENETIC TESTING; HUMANS; IRAN; MALE; MUTATION, MISSENSE;

EID: 84857609229     PISSN: 10760296     EISSN: 19382723     Source Type: Journal    
DOI: 10.1177/1076029611412363     Document Type: Article

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