Further evidence that mutations in INScan be a rare cause of Maturity-Onset Diabetes of the Young (MODY)-Reference-Cited by-同舟云学术

Further evidence that mutations in INScan be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

Published:2010-03-12 Issue:1 Volume:11 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Boesgaard Trine W,Pruhova Stepanka,Andersson Ehm A,Cinek Ondrej,Obermannova Barbora,Lauenborg Jeannet,Damm Peter,Bergholdt Regine,Pociot Flemming,Pisinger Charlotta,Barbetti Fabrizio,Lebl Jan,Pedersen Oluf,Hansen Torben

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-11-42.pdf

Reference9 articles.

1. Bonfanti R, Colombo C, Nocerino V, et al: Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodies. Diabetes care. 2009, 32: 123-125. 10.2337/dc08-0783.

2. Colombo C, Porzio O, Liu M, et al: Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus. J Clin Invest. 2008, 118: 2148-2156.

3. Edghill EL, Flanagan SE, Patch AM, et al: Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood. Diabetes. 2008, 57: 1034-1042. 10.2337/db07-1405.

4. Støy J, Edghill EL, Flanagan SE, et al: Insulin gene mutations as a cause of permanent neonatal diabetes. Proceedings of the National Academy of Sciences. 2007, 104: 15040-15044. 10.1073/pnas.0707291104.

5. Murphy R, Ellard S, Hattersley AT: Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes. Nat Clin Pract Endocrinol Metab. 2008, 4: 200-213. 10.1038/ncpendmet0778.

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