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

by Achour Abdellatif, Zellama Dorsaf, Omezzine Asma, Abroug Saoussen, Mbarek Ibtihel, Harbi Abdelaziz, Bouslama Ali
Published 2011-05-01