Two novel frame shift, recurrent and de novo mutations in the ITGB2 (CD18) gene causing leukocyte adhesion deficiency in a highly inbred North African population

por Fathallah, D. M, Jamal, T., Barbouche, M. R, Bejaoui, M., Hariz, M. Ben, Dellagi, K.
Publicado 2001

Novel gene mutations underlying two new cases of ALPS 0 syndrome

por Barbouche, MR, Ben Mustapha, I, Dhouib, N, Mattoussi, N, Riahi, R, Larguèche, B, Ben Becheur, S, Béjaoui, M
Publicado 2011

Molecular basis of primary immune deficiencies in a highly inbred population

por Barbouche, MR, Ben Mustapha, I, Mellouli, F, Dhouib, N, Riahi, R, Ben Farhat, K, Ouadhani, H, Bejaoui, M, Dellagi, K
Publicado 2011