A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype–phenotype correlation
Crossref DOI link: https://doi.org/10.1007/s12041-016-0676-4
Published Online: 2016-08-20
Published Print: 2016-09
Update policy: https://doi.org/10.1007/springer_crossmark_policy
M’DIMEGH, SAOUSSEN
AQUAVIVA-BOURDAIN, CÉCILE
OMEZZINE, ASMA
M’BAREK, IBTIHEL
SOUCHE, GENEVIÉVE
ZELLAMA, DORSAF
ABIDI, KAMEL
ACHOUR, ABDELATTIF
GARGAH, TAHAR
ABROUG, SAOUSSEN
BOUSLAMA, ALI
License valid from 2016-08-20