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

• Үндсэн зохиолчид: Elmahmoudi Hejer (Зохиогч), Ben-lakhal Fatma (Зохиогч), Elborji Wijden (Зохиогч), Jlizi Asma (Зохиогч), Zahra Kaouther (Зохиогч), Sassi Rim (Зохиогч), Zorgan Moez (Зохиогч), Meddeb Balkis (Зохиогч), Elgaaied Ben Ammar Amel (Зохиогч), Gouider Emna (Зохиогч)
• Формат: Ном
• Хэвлэсэн: BMC, 2012-08-01T00:00:00Z.
• Нөхцлүүд: article
• Онлайн хандалт: Connect to this object online.

<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...