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Genotype-phenotype correlation of K(ATP) channel gene defects causing permanent neonatal diabetes in Indian patients.

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2021 Feb Others S Gopi, B Kavitha, S Kanthimathi, A Kannan… - … Diabetes, 2021 - Wiley Online Library

Full Author : ['Gopi, Sundaramoorthy', 'Kavitha, Babu', 'Kanthimathi, Sekar', 'Kannan, Alagarsamy', 'Kumar, Rakesh', 'Joshi, Rajesh', 'Kanodia, Swati', 'Arya, Archana Dayal', 'Pendsey, Sanket', 'Pendsey, Sharad', 'Raghupathy, Palany', 'Mohan, Viswanathan', 'Radha, Venkatesan']
Journal Title : Pediatric diabetes
Chapter : Section3
Journal Year : 2021
Cited by : 9.0

BACKGROUND: There are very few reports pertaining to Indian patients with neonatal diabetes mellitus (NDM). Activating or gain of function mutations of K(ATP) channel genes namely KCNJ11 and ABCC8 are most predominant cause of permanent neonatal diabetes ..... Read More

Keywords : ["katp channel gene defect cause permanent neonatal diabetes", "indian patient", "genotypephenotype correlation"]
PubMed Link : https://onlinelibrary.wiley.com/doi/abs/10.1111/pedi.13109
Google Scholar Link : https://scholar.google.com/scholar?cites=116851391148001053&as_sdt=2005&sciodt=0,5&hl=en&num=20