![](/img/cover-not-exists.png)
SelectedAGXTgene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria
Ibtihel Benhaj Mbarek, Saoussen Abroug, Asma Omezzine, Dorsaf Zellama, Abdellatif Achour, Abdelaziz Harbi, Ali BouslamaVolume:
12
Language:
english
DOI:
10.1186/1471-2369-12-25
Date:
December, 2011
File:
PDF, 230 KB
english, 2011