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	1.	HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients. [electronic resource] by M'dimegh, Saoussen Aquaviva-Bourdain, Cécile Omezzine, Asma Souche, Geneviéve M'barek, Ibtihel Abidi, Kamel Gargah, Tahar Abroug, Saoussen Bouslama, Ali Producer: 20171227 In: Journal of clinical laboratory analysis vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype-phenotype correlation. [electronic resource] by 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 Producer: 20170329 In: Journal of genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of a novel AGXT gene mutation in primary hyperoxaluria after kidney transplantation failure. [electronic resource] by M'dimegh, Saoussen Omezzine, Asma Hamida-Rebai, Mériam Ben Aquaviva-Bourdain, Cécile M'barek, Ibtihel Sahtout, Wissal Zellama, Dorsaf Souche, Geneviéve Achour, Abdellatif Abroug, Saoussen Bouslama, Ali Producer: 20180116 In: Transplant immunology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1. [electronic resource] by M'dimegh, Saoussen Omezzine, Asma M'barek, Ibtihel Moussa, Amira Mabrouk, Sameh Kaarout, Hayet Souche, Geneviéve Chemli, Jalel Aloui, Sabra Aquaviva-Bourdain, Cécile Achour, Abdellatif Abroug, Saoussen Bouslama, Ali Producer: 20170530 In: Annals of human genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)