Your browser doesn't support javascript.
loading
Detection of a novel mutation in a Tunisian child with polycystic kidney disease.
Abdelwahed, Mayssa; Hilbert, Pascale; Ahmed, Asma; Dey, Mouna; Kamoun, Hassen; Ammar-Keskes, Leila; Belguith, Neïla.
Affiliation
  • Abdelwahed M; Laboratory of Human Molecular Genetics, Faculty of Medicine, University of Sfax, Sfax, Tunisia.
  • Hilbert P; Center of Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium.
  • Ahmed A; Nephrology and Hemodialyse Department, Mohamed Ben Sassi Hospital, Gabes, Tunisia.
  • Dey M; Nephrology and Hemodialyse Department, Mohamed Ben Sassi Hospital, Gabes, Tunisia.
  • Kamoun H; Medical Genetics Department, HediChaker Hospital, Sfax, Tunisia.
  • Ammar-Keskes L; Laboratory of Human Molecular Genetics, Faculty of Medicine, University of Sfax, Sfax, Tunisia.
  • Belguith N; Laboratory of Human Molecular Genetics, Faculty of Medicine, University of Sfax, Sfax, Tunisia.
IUBMB Life ; 72(8): 1799-1806, 2020 08.
Article in En | MEDLINE | ID: mdl-32472977
Subject(s)
Key words
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycystic Kidney, Autosomal Dominant / Genetic Predisposition to Disease / TRPP Cation Channels Type of study: Diagnostic_studies / Prognostic_studies Aspects: Patient_preference Limits: Child, preschool / Female / Humans Country/Region as subject: Africa Language: En Journal: IUBMB Life Year: 2020 Document type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycystic Kidney, Autosomal Dominant / Genetic Predisposition to Disease / TRPP Cation Channels Type of study: Diagnostic_studies / Prognostic_studies Aspects: Patient_preference Limits: Child, preschool / Female / Humans Country/Region as subject: Africa Language: En Journal: IUBMB Life Year: 2020 Document type: Article