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