Your browser doesn't support javascript.
loading
Mutational analysis in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD): Identification of five mutations in the PKD1 gene.
Abdelwahed, Mayssa; Hilbert, Pascale; Ahmed, Asma; Mahfoudh, Hichem; Bouomrani, Salem; Dey, Mouna; Hachicha, Jamil; Kamoun, Hassen; Keskes-Ammar, Leila; Belguith, Neïla.
Affiliation
  • Abdelwahed M; Laboratory of Human Molecular Genetics, Faculty of Medicine, Magida Boulila Street, 3029 Sfax, University of Sfax, Tunisia. Electronic address: abdelwahed.mayssa@yahoo.fr.
  • Hilbert P; Center of Human Genetics, Institute of Pathology and Genetics, Biopark Charleroi Brussels South. Rue Adrienne Bolland 8. Aéropole de Gosselies, B - 6041 Gosselies, Belgium.
  • Ahmed A; Nephrology and Hemodialyse department of Mohamed Ben Sassi Hospital, Route EbenKhaldoun, Mtorrech, Gabes 6014, Tunisia.
  • Mahfoudh H; Nephrology Department of HediChaker Hospital, Route El Ain, Sfax 3089, Tunisia.
  • Bouomrani S; General Medicine department of Military Hospital, Route Mongi Slim, Gabes 6000, Tunisia.
  • Dey M; Nephrology and Hemodialyse department of Mohamed Ben Sassi Hospital, Route EbenKhaldoun, Mtorrech, Gabes 6014, Tunisia.
  • Hachicha J; Nephrology Department of HediChaker Hospital, Route El Ain, Sfax 3089, Tunisia.
  • Kamoun H; Medical Genetics Department of HediChaker Hospital, Route El Ain, Sfax 3089, Tunisia.
  • Keskes-Ammar L; Laboratory of Human Molecular Genetics, Faculty of Medicine, Magida Boulila Street, 3029 Sfax, University of Sfax, Tunisia.
  • Belguith N; Laboratory of Human Molecular Genetics, Faculty of Medicine, Magida Boulila Street, 3029 Sfax, University of Sfax, Tunisia; Medical Genetics Department of HediChaker Hospital, Route El Ain, Sfax 3089, Tunisia.
Gene ; 671: 28-35, 2018 Sep 10.
Article in En | MEDLINE | ID: mdl-29860066
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 / TRPP Cation Channels / Mutation Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Adult / Aged / Child / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: Gene Year: 2018 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 / TRPP Cation Channels / Mutation Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Adult / Aged / Child / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: Gene Year: 2018 Document type: Article