Zobrazeno 1 - 4
of 4
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff396de0b8279edb0a1bca82e8aed24b
https://doi.org/10.1111/ahg.12178
https://doi.org/10.1111/ahg.12178
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2f45f3905d4b4a7e4b5f1affd326d23
https://pubmed.ncbi.nlm.nih.gov/27935012
https://pubmed.ncbi.nlm.nih.gov/27935012
Autor:
M'dimegh, Saoussen1 sawsen_mdimegh@live.fr, Omezzine, Asma1, M'barek, Ibtihel1, Moussa, Amira1, Mabrouk, Sameh1, Kaarout, Hayet2, Souche, Geneviéve3, Chemli, Jalel4, Aloui, Sabra5, Aquaviva‐Bourdain, Cécile3, Achour, Abdellatif6, Abroug, Saoussen4, Bouslama, Ali1
Publikováno v:
Annals of Human Genetics. Jan2017, Vol. 81 Issue 1, p1-10. 10p.
Publikováno v:
NDT Plus; Jun2010 Supplement 3, Vol. 3 Issue suppl_3, piii303-iii547, 1p