FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome-Reference-Cited by-同舟云学术

FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome

Published:2017-11-29 Issue:3 Volume:19 Page:388-392
ISSN:1399-543X
Container-title:Pediatric Diabetes
language:en
Short-container-title:Pediatr Diabetes

Author:

Hwang Jessica L¹,Park Soo-Young¹,Ye Honggang¹,Sanyoura May¹,Pastore Ashley N¹,Carmody David¹,del Gaudio Daniela²,Wilson Janna F³,Hanis Craig L⁴,Liu Xiaoming⁴,Atzmon Gil⁵,Glaser Benjamin⁶,Philipson Louis H¹,Greeley Siri Atma W¹^ORCID,

Affiliation:

1. Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism and Kovler Diabetes Center; The University of Chicago; Chicago Illinois

2. Department of Human Genetics; The University of Chicago; Chicago Illinois

3. Women's and Children's Hospital; Lafayette Louisiana

4. Genetics Center; University of Texas Health Science Center at Houston; Houston Texas

5. Departments of Medicine and Genetics; Albert Einstein College of Medicine; New York City New York

6. Department of Internal Medicine; Hadassah-Hebrew Medical Center; Jerusalem Israel

Funder

Juvenile Diabetes Research Foundation International

American Diabetes Association

National Institute of Diabetes and Digestive and Kidney Diseases

National Center for Advancing Translational Sciences

National Human Genome Research Institute

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health,Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pedi.12612/fullpdf

Reference13 articles.

1. The diagnosis and management of monogenic diabetes in children and adolescents;Hattersley;Pediatr Diabetes,2009

2. Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment;Greeley;Curr Diab Rep,2011

3. The immunogenetics of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome;d'Hennezel;J Med Genet,2012

4. Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome;Wildin;J Med Genet,2002

5. Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes;Rubio-Cabezas;Diabetes Care,2009

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