Guipponi M, Masclaux F, Sloan-Béna F, Di Sanza C, Özbek N, Peyvandi F, Menegatti M, Casini A, Malbora B, Neerman-Arbez M. A homozygous duplication of the <I>FGG</i> exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family. haematol [Internet]. 2022May1 [cited 2024Apr.25];107(5):1064-71. Available from: https://haematologica.org/article/view/haematol.2021.278945