Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children-Reference-Cited by-同舟云学术

Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children

Published:2012-08-20 Issue:5 Volume:83 Page:439-445
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Jahnavi S¹,Poovazhagi V²,Mohan V,Bodhini D¹,Raghupathy P³,Amutha A⁴,Suresh Kumar P⁵,Adhikari P⁶,Shriraam M⁷,Kaur T⁸,Das AK⁹,Molnes J¹⁰,Njolstad PR¹¹,Unnikrishnan R¹²,Radha V¹

Affiliation:

1. Department of Molecular Genetics; Madras Diabetes Research Foundation; Chennai; Tamil Nadu; India

2. Department of Pediatrics; Institute of Child Health and Hospital for Children; Chennai; Tamil Nadu; India

3. Department of Pediatrics; Sagar Hospital; Bangalore; Karnataka; India

4. Department of Epidemiology; Madras Diabetes Research Foundation; Chennai; Tamil Nadu; India

5. Department of Medicine; Diabcare India Diabetes center; Kozhikodu; Kerala; India

6. Department of Medicine; Kasturba Medical College; Mangalore; Karnataka; India

7. Department of Medicine; Apollo Children's Hospitals; Chennai; Tamil Nadu; India

8. Department of NCD; Indian Council of Medical Research; New Delhi; Delhi; India

9. Department of Medicine; Jawaharlal Institute of Postgraduate Medical Education and Research; Puducherry; Tamilnadu; India

10. Department of Pediatrics; Haukeland University Hospital; Bergen; Hordaland; Norway

11. Department of Clinical Medicine; University of Bergen; Bergen; Norway

12. Department of Diabetology; Dr. Mohan's Diabetes Specialities Centre; Chennai; Tamil Nadu; India

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2012.01939.x/fullpdf

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3. Rfx6 directs islet formation and insulin production in mice and humans;Smith;Nature,2010

4. GATA6 haploinsufficiency causes pancreatic agenesis in humans;Allen;Nat Genet,2011

5. Activating mutations in the ABCC8 gene in neonatal diabetes mellitus;Babenko;N Engl J Med,2006

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