Small insertion (c.869insC) within F13A gene is dominant in Tunisian patients with inherited FXIII deficiency due to ancient founder effect
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| Veröffentlicht in: | Haemophilia : the official journal of the World Federation of Hemophilia 2009-09, Vol.15 (5), p.1176-1179 |
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| container_end_page | 1179 |
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| container_title | Haemophilia : the official journal of the World Federation of Hemophilia |
| container_volume | 15 |
| creator | EL MAHMOUDI, H. AMOR, M. B. GOUIDER, E. HORCHANI, R. HAFSIA, R. FADHLAOUI, K. MEDDEB, B. HAFSIA, A. AMMAR EL GAAIED, A. B. |
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| doi_str_mv | 10.1111/j.1365-2516.2009.02053.x |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1351-8216 |
| ispartof | Haemophilia : the official journal of the World Federation of Hemophilia, 2009-09, Vol.15 (5), p.1176-1179 |
| issn | 1351-8216 1365-2516 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_733314314 |
| source | MEDLINE; Wiley Journals |
| subjects | Adult Factor XIII Deficiency - genetics Female Founder Effect Genotype Humans Male Phenotype Postpartum Hemorrhage - prevention & control Pregnancy Tunisia |
| title | Small insertion (c.869insC) within F13A gene is dominant in Tunisian patients with inherited FXIII deficiency due to ancient founder effect |
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