Identification of two novel missense mutations causing severe factor XIII deficiency

Haemophilia

Volumn 21, Issue 3, 2015, Pages e253-e256

  Handrkova, H ^a,b   Borhany, M ^c   Schroeder, V ^a,b   Fatima, N ^c   Hussain, A ^c   Shamsi, T ^c   Kohler, H P ^a,b,d  

^a UNIVERSITY OF BERN   (Switzerland)

^b UNIVERSITY OF BERN   (Switzerland)

^c National Institute of Blood Disease and Bone Marrow Transplantation (NIBD)   (Pakistan)

^d Spital Netz Bern ^*  (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

TRANEXAMIC ACID; BLOOD CLOTTING FACTOR 13;

ALPHA HELIX; BLOOD CLOTTING FACTOR 13 DEFICIENCY; CLINICAL EXAMINATION; CRYOPRECIPITATE; HUMAN; HYDROGEN BOND; INCIDENCE; LETTER; MISSENSE MUTATION; PATIENT CARE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; ADOLESCENT; CASE REPORT; CHEMISTRY; FACTOR XIII DEFICIENCY; FEMALE; GENETICS; HOMOZYGOTE; MALE; YOUNG ADULT;

ADOLESCENT; FACTOR XIII; FACTOR XIII DEFICIENCY; FEMALE; HOMOZYGOTE; HUMANS; MALE; MUTATION, MISSENSE; YOUNG ADULT;

EID: 84928828080     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/hae.12663     Document Type: Letter

References (9)

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