Continued lessons from theINSgene: an intronic mutation causing diabetes through a novel mechanism-Reference-Cited by-同舟云学术

Continued lessons from theINSgene: an intronic mutation causing diabetes through a novel mechanism

Published:2015-06-22 Issue:9 Volume:52 Page:612-616
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Carmody David,Park Soo-Young,Ye Honggang,Perrone Marie E,Alkorta-Aranburu G,Highland Heather M,Hanis Craig L,Philipson Louis H,Bell Graeme I,Greeley Siri Atma W

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference20 articles.

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2. Insulin gene mutations as a cause of permanent neonatal diabetes;Støy;Proc Natl Acad Sci USA,2007

3. Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene;Støy;Rev Endocr Metab Disord,2010

4. Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus;Colombo;J Clin Invest,2008

5. Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted;Park;Biochem Biophys Res Commun,2010

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