Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria

por Mbarek, Ibtihel Benhaj, Abroug, Saoussen, Omezzine, Asma, Zellama, Dorsaf, Achour, Abdellatif, Harbi, Abdelaziz, Bouslama, Ali
Publicado 2011

Unusual clinical outcome of primary Hyperoxaluria type 1 in Tunisian patients carrying 33_34InsC mutation

por Mbarek, Ibtihel Benhaj, Mdimeg, Saoussen, Moussa, Amira, Zellama, Dorsaf, Kaarout, Hayat, Abdelmoula, Jaouida, Achour, Abdellatif, Abroug, Saoussen, Omezzine, Asma, Bouslama, Ali
Publicado 2017