Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiency-Reference-Cited by-同舟云学术

Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiency

Published:2014-11-18 Issue:2 Volume:17 Page:153-159
ISSN:1399-543X
Container-title:Pediatric Diabetes
language:en
Short-container-title:Pediatr Diabetes

Author:

Hogendorf Anna¹,Lipska-Zietkiewicz Beata S.²,Szadkowska Agnieszka¹,Borowiec Maciej¹³,Koczkowska Magdalena²,Trzonkowski Piotr⁴,Drozdz Izabela¹,Wyka Krystyna¹,Limon Janusz²,Mlynarski Wojciech¹

Affiliation:

1. Department of Pediatrics, Oncology, Hematology and Diabetology; Medical University of Lodz; Lodz Poland

2. Department of Biology and Genetics; Medical University of Gdansk; Gdansk Poland

3. Department of Clinical Genetics; Medical University of Lodz; Lodz Poland

4. Clinical Immunology and Transplantology Unit at the Department of Immunology; Medical University of Gdansk; Gdansk Poland

Funder

Fundacja na rzecz Nauki Polskiej

Narodowe Centrum Nauki

Diabetes Poland grant (AH)

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pedi.12235/fullpdf

Reference37 articles.

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3. Positional cloning of the APECED gene;Nagamine;Nat Genet,1997

4. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3;Benett;Nat Genet,2001

5. The diagnosis and management of monogenic diabetes in children and adolescents;Rubio-Cabezas;Pediatr Diabetes,2014

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