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Identification of genetic defects underlying FVII deficiency in 10 patients belonging to eight unrelated families of the North provinces from Tunisia
Inherited factor VII (FVII) deficiency is a rare disorder characterized by a bleeding phenotype varying from mild to severe. To date, more than 200 mutations have been described along the F7 gene encoding for FVII. The aim of this study was the identification of genetic defects underlying FVII defic...
Autores principales: | Elmahmoudi, Hejer, Ben-lakhal, Fatma, Elborji, Wijden, Jlizi, Asma, Zahra, Kaouther, Sassi, Rim, Zorgan, Moez, Meddeb, Balkis, Elgaaied Ben Ammar, Amel, Gouider, Emna |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526404/ https://www.ncbi.nlm.nih.gov/pubmed/22873696 http://dx.doi.org/10.1186/1746-1596-7-92 |
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