Insulin gene mutations linked to permanent neonatal diabetes mellitus in Indian population

Neonatal diabetes mellitus (NDM) is a rare monogenic disorder of pancreatic beta cell mass and/or function. In the present study we aimed to evaluate the INS gene mutations in a cohort of children with Permanent Neonatal Diabetes Mellitus (PNDM) and to explore the clinical and genetic characteristic...

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Veröffentlicht in:	Journal of diabetes and its complications 2021-12, Vol.35 (12), p.108022-108022, Article 108022
Hauptverfasser:	Gopi, Sundaramoorthy, Gowri, Palanisamy, Panda, Jayant Kumar, Sathyanarayana, Santhosh Olety, Gupta, Sunil, Chandru, Sundaramoorthy, Chandni, Radhakrishnan, Raghupathy, Palany, Dayal, Devi, Mohan, Viswanathan, Radha, Venkatesan
Format:	Artikel
Sprache:	eng
Schlagworte:	Antibodies Asian Indians Birth weight Diabetes Diabetes Mellitus - diagnosis Diabetes Mellitus - epidemiology Diabetes Mellitus - genetics Endoplasmic reticulum Female Genes Genomes Genomics Glucose Humans India - epidemiology Infant Infant, Newborn INS gene mutations Insulin Insulin - genetics Insulin treatment Male Mutation Newborn babies Pedigree Peptides Permanent neonatal diabetes mellitus Precision medicine Proteins Sequence Analysis, DNA South Asians
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