Congenital secretory diarrhoea caused by activating germline mutations inGUCY2C-Reference-Cited by-同舟云学术

Congenital secretory diarrhoea caused by activating germline mutations inGUCY2C

Published:2015-05-20 Issue:8 Volume:65 Page:1306-1313
ISSN:0017-5749
Container-title:Gut
language:en
Short-container-title:Gut

Author:

Müller Thomas,Rasool Insha,Heinz-Erian Peter,Mildenberger Eva,Hülstrunk Christian,Müller Andreas,Michaud Laurent,Koot Bart G P,Ballauff Antje,Vodopiutz Julia,Rosipal Stefan,Petersen Britt-Sabina,Franke Andre,Fuchs Irene,Witt Heiko,Zoller Heinz,Janecke Andreas R,Visweswariah Sandhya S

Publisher

BMJ

Subject

Gastroenterology

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3. Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea;Heinz-Erian;Am J Hum Genet,2009

4. Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form;Salomon;Human Genet,2014

5. Familial diarrhea syndrome caused by an activating GUCY2C mutation;Fiskerstrand;N Engl J Med,2012

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