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Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1.
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.
Afiliação
  • M'dimegh S; Biochemistry Department, Sahloul University Hospital, Sousse, Tunisia.
  • Omezzine A; Biochemistry Department, Sahloul University Hospital, Sousse, Tunisia.
  • M'barek I; Biochemistry Department, Sahloul University Hospital, Sousse, Tunisia.
  • Moussa A; Biochemistry Department, Sahloul University Hospital, Sousse, Tunisia.
  • Mabrouk S; Biochemistry Department, Sahloul University Hospital, Sousse, Tunisia.
  • Kaarout H; Internal Medicine A Department, Charles Nicolle University Hospital, Tunis, Tunisia.
  • Souche G; Laboratory of Inborn Metabolic Diseases, Centre de Biologie Est, Hospices Civils de Lyon, Lyon, France.
  • Chemli J; Pediatric Department, Sahloul University Hospital, Sousse, Tunisia.
  • Aloui S; Nephrology Department, Fatouma Bourguiba University Hospital, Monastir, Tunisia.
  • Aquaviva-Bourdain C; Laboratory of Inborn Metabolic Diseases, Centre de Biologie Est, Hospices Civils de Lyon, Lyon, France.
  • Achour A; Nephrology Department, Sahloul University Hospital, Sousse, Tunisia.
  • Abroug S; Pediatric Department, Sahloul University Hospital, Sousse, Tunisia.
  • Bouslama A; Biochemistry Department, Sahloul University Hospital, Sousse, Tunisia.
Ann Hum Genet ; 81(1): 1-10, 2017 Jan.
Article em En | MEDLINE | ID: mdl-27935012
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperoxalúria Primária / Transaminases Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperoxalúria Primária / Transaminases Idioma: En Ano de publicação: 2017 Tipo de documento: Article