Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect.

MLA

Louhichi, Nacim, et al. “Congenital Factor XIII Deficiency Caused by Two Mutations in Eight Tunisian Families: Molecular Confirmation of a Founder Effect.” Annals of Hematology, vol. 89, no. 5, May 2010, pp. 499–504. EBSCOhost, https://doi.org/10.1007/s00277-009-0863-y.

APA

Louhichi, N., Medhaffar, M., HadjSalem, I., Mkaouar-Rebai, E., Fendri-Kriaa, N., Kanoun, H., Yaïch, F., Souissi, T., Elloumi, M., & Fakhfakh, F. (2010). Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect. Annals of Hematology, 89(5), 499–504. https://doi.org/10.1007/s00277-009-0863-y

Chicago

Louhichi, Nacim, Moez Medhaffar, Ikhlass HadjSalem, Emna Mkaouar-Rebai, Nourhene Fendri-Kriaa, Houda Kanoun, Firas Yaïch, Tawfik Souissi, Moez Elloumi, and Faiza Fakhfakh. 2010. “Congenital Factor XIII Deficiency Caused by Two Mutations in Eight Tunisian Families: Molecular Confirmation of a Founder Effect.” Annals of Hematology 89 (5): 499–504. doi:10.1007/s00277-009-0863-y.