Genotype/phenotype correlation in FHHNC caused by mutations in either CLDN16 or CLDN19: long-term follow-up in 125 patients
Haisch L, Schlingmann KP, Tasic V, Al-Attrach I, Cochat P, Sikora P, Ariceta G, Kari J, Dittrich K, Konrad M
Research article (journal)Details about the publication
Journal: Pediatric Nephrology (Pediatr Nephrol)
Volume: 26
Issue: 9
Page range: 1573-1574
Status: Published
Release year: 2011
Language in which the publication is written: English
Authors from the University of Münster
| Haisch, Lea | University Children's Hospital - Department for General Paediatrics |
| Konrad, Martin | University Children's Hospital - Department for General Paediatrics |
| Schlingmann, Karl Peter | University Children's Hospital - Department for General Paediatrics |