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Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.
Borhany, M; Handrkova, H; Cairo, A; Schroeder, V; Fatima, N; Naz, A; Amanat, S; Shamsi, T; Peyvandi, F; Kohler, H P.
Affiliation
  • Borhany M; Department of Haematology, Haemostasis & Thrombosis, National Institute of Blood Disease and Bone Marrow Transplantation (NIBD), Karachi, Pakistan.
Haemophilia ; 20(4): 568-74, 2014 Jul.
Article in En | MEDLINE | ID: mdl-24329762
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pedigree / Factor XIII / DNA Mutational Analysis / Factor XIII Deficiency / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Haemophilia Year: 2014 Document type: Article
Fulltext
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pedigree / Factor XIII / DNA Mutational Analysis / Factor XIII Deficiency / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Haemophilia Year: 2014 Document type: Article