Significance of Molecular Testing for Congenital Chloride Diarrhea-Reference-Cited by-同舟云学术

Significance of Molecular Testing for Congenital Chloride Diarrhea

Published:2011-07 Issue:1 Volume:53 Page:48-54
ISSN:0277-2116
Container-title:Journal of Pediatric Gastroenterology & Nutrition
language:en
Short-container-title:

Author:

Lechner Silvia,Ruemmele Frank M,Zankl Andreas,Lausch Ekkehart,Huber Wolf-Dietrich,Mihatsch Walter,Phillips Alan D,Lewindon Peter,Querfeld Uwe,Heinz-Erian Peter,Müller Thomas,Janecke Andreas R

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Pediatrics, Perinatology, and Child Health

Reference37 articles.

1. Review article: the clinical management of congenital chloride diarrhoea;Wedenoja;Aliment Pharmacol Ther,2010

2. Colonic electrolyte transport in health and in congenital chloride diarrhea;Holmberg;J Clin Invest,1975

3. Congenital diarrheal disorders: improved understanding of gene defects is leading to advances in intestinal physiology and clinical management;Canani;J Pediatr Gastroenterol Nutr,2010

4. A novel homozygous SLC26A3 nonsense mutation in a Tyrolean girl with congenital chloride diarrhea;Heinz-Erian;J Pediatr Gastroenterol Nutr,2008

5. Mutations of the down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea;Hoglund;Nat Genet,1996

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