Molecular analysis of sixteen unrelated factor XIIIA deficient families from south-east of Iran [4]

British Journal of Haematology

Volumn 140, Issue 5, 2008, Pages 581-584

  Trinh, Chi H ^a   Sh ElSayed, Walid ^b   Eshghi, Peyman ^c   Miri Moghaddam, Ebrahim ^d   Zadeh Vakili, Azita ^d   Markham, Alexander F ^b   Anwar, Rashida ^b  

^a UNIVERSITY OF LEEDS   (United Kingdom)

^b UNIVERSITY OF LEEDS   (United Kingdom)

^c SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d ZAHEDAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Founder mutation; FXIIIA; Modelling; Protein structure; Transglutaminases

Indexed keywords

BLOOD CLOTTING FACTOR 13A;

BLOOD CLOTTING FACTOR 13 DEFICIENCY; CONSANGUINEOUS MARRIAGE; GENE AMPLIFICATION; GENE MUTATION; HOMOZYGOSITY; HUMAN; IRAN; LETTER; MORBIDITY; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL;

FACTOR XIII DEFICIENCY; FACTOR XIIIA; HUMANS; MODELS, MOLECULAR; MUTATION;

EID: 39049106677     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2007.06963.x     Document Type: Letter

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