Congenital Proprotein Convertase 1/3 Deficiency Causes Malabsorptive Diarrhea and Other Endocrinopathies in a Pediatric Cohort-Reference-Cited by-同舟云学术

Congenital Proprotein Convertase 1/3 Deficiency Causes Malabsorptive Diarrhea and Other Endocrinopathies in a Pediatric Cohort

Published:2013-07 Issue:1 Volume:145 Page:138-148
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Martín Martín G.,Lindberg Iris,Solorzano–Vargas R. Sergio,Wang Jiafang,Avitzur Yaron,Bandsma Robert,Sokollik Christiane,Lawrence Sarah,Pickett Lindsay A.,Chen Zijun,Egritas Odul,Dalgic Buket,Albornoz Valeria,de Ridder Lissy,Hulst Jessie,Gok Faysal,Aydoğan Ayşen,Al–Hussaini Abdulrahman,Gok Deniz Engin,Yourshaw Michael,Wu S. Vincent,Cortina Galen,Stanford Sara,Georgia Senta

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

California Institute of Regenerative Medicine

National Institute on Drug Abuse

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference28 articles.

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

2. Mutant neurogenin-3 in congenital malabsorptive diarrhea;Wang;N Engl J Med,2006

3. Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene;Jackson;Nat Genet,1997