Identification of genetic defects underlying FVII deficiency in 10 patients belonging to eight unrelated families of the North provinces from Tunisia

Identification of genetic defects underlying FVII deficiency in 10 patients belonging to eight unrelated families of the North provinces from Tunisia

<p>Abstract</p> <p>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 <it>F7</it> gene encoding for FVII. The aim of this study was t...

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Main Authors: Elmahmoudi Hejer (Author), Ben-lakhal Fatma (Author), Elborji Wijden (Author), Jlizi Asma (Author), Zahra Kaouther (Author), Sassi Rim (Author), Zorgan Moez (Author), Meddeb Balkis (Author), Elgaaied Ben Ammar Amel (Author), Gouider Emna (Author)
Format: Book
Published: BMC, 2012-08-01T00:00:00Z.
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