First report of molecular diagnosis of Tunisian hemophiliacs A: Identification of 8 novel causative mutations

• Автори: Elmahmoudi Hejer (Автор), Khodjet- (Автор), Wigren Edvard (Автор), Jlizi Asma (Автор), Zahra Kaouther (Автор), Pellechia Dorothé (Автор), Vinciguerra Christine (Автор), Meddeb Balkis (Автор), Elggaaied Amel Ben (Автор), Gouider Emna (Автор)
• Формат: Книга
• Опубліковано: BMC, 2012-08-01T00:00:00Z.
• Предмети: article
• Онлайн доступ: Connect to this object online.

<p>Abstract</p> <p>Introduction</p> <p>Hemophilia A is an X linked recessive hemorrhagic disorder caused by mutations in the <it>F8</it> gene that lead to qualitative and/or quantitative deficiencies of coagulation factor VIII (FVIII). Molecular diagnosis of...