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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
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

Internet

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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