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pro vyhledávání: '"Hayet Kaarout"'
Autor:
Hayet Kaarout, Jalel Chemli, Abdellatif Achour, Amira Moussa, Asma Omezzine, Saoussen Abroug, Ali Bouslama, Geneviéve Souche, Sabra Aloui, Saoussen M'dimegh, Ibtihel M'barek, Cécile Aquaviva-bourdain, Sameh Mabrouk
Publikováno v:
Annals of Human Genetics. 81:1-10
Background Primary hyperoxaluria type 1 (PH1) is an autosomal recessive metabolic disorder caused by inherited mutations in the AGXT gene encoding liver peroxisomal alanine:glyoxylate aminotransferase (AGT). PH1 is a clinically and genetically hetero
Autor:
Saoussen, M'dimegh, Asma, Omezzine, Ibtihel, M'barek, Amira, Moussa, Sameh, Mabrouk, Hayet, Kaarout, Geneviéve, Souche, Jalel, Chemli, Sabra, Aloui, Cécile, Aquaviva-Bourdain, Abdellatif, Achour, Saoussen, Abroug, Ali, Bouslama
Publikováno v:
Annals of human genetics. 81(1)
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive metabolic disorder caused by inherited mutations in the AGXT gene encoding liver peroxisomal alanine:glyoxylate aminotransferase (AGT). PH1 is a clinically and genetically heterogeneous dis