[Clinical Features and INS Mutations of an Infant with Neonatal Diabetes Mellitus]
Overview
Overview
Authors
Authors
Affiliations
Affiliations
Soon will be listed here.
References
1.
Stoy J, Edghill E, Flanagan S, Ye H, Paz V, Pluzhnikov A
. Insulin gene mutations as a cause of permanent neonatal diabetes. Proc Natl Acad Sci U S A. 2007; 104(38):15040-4.
PMC: 1986609.
DOI: 10.1073/pnas.0707291104.
View
2.
Rajan S, Eames S, Park S, Labno C, Bell G, Prince V
. In vitro processing and secretion of mutant insulin proteins that cause permanent neonatal diabetes. Am J Physiol Endocrinol Metab. 2009; 298(3):E403-10.
PMC: 2838531.
DOI: 10.1152/ajpendo.00592.2009.
View
3.
Park S, Ye H, Steiner D, Bell G
. Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted. Biochem Biophys Res Commun. 2009; 391(3):1449-54.
PMC: 2817945.
DOI: 10.1016/j.bbrc.2009.12.090.
View
4.
Nour M, Pacaud D
. Height augmentation in 11β-hydroxylase deficiency congenital adrenal hyperplasia. Int J Pediatr Endocrinol. 2015; 2015(1):12.
PMC: 4432823.
DOI: 10.1186/s13633-015-0008-0.
View