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	1.	Functional characterization of activating mutations in the sulfonylurea receptor 1 (ABCC8) causing neonatal diabetes mellitus in Asian Indian children. [electronic resource] by Balamurugan, Kandasamy Kavitha, Babu Yang, Zhongying Mohan, Viswanathan Radha, Venkatesan Shyng, Show-Ling Producer: 20200323 In: Pediatric diabetes vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Identification and molecular characterization of HNF1B gene mutations in Indian diabetic patients with renal abnormalities. [electronic resource] by Kanthimathi, Sekar Balamurugan, Kandasamy Mohan, Viswanathan Shanthirani, Coimbatore Subramaniyam Gayathri, Vijay Radha, Venkatesan Producer: 20150529 In: Annals of human genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Glucokinase gene mutations (MODY 2) in Asian Indians. [electronic resource] by Kanthimathi, Sekar Jahnavi, Suresh Balamurugan, Kandasamy Ranjani, Harish Sonya, Jagadesan Goswami, Soumik Chowdhury, Subhankar Mohan, Viswanathan Radha, Venkatesan Producer: 20141128 In: Diabetes technology & therapeutics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia. [electronic resource] by Jahnavi, Suresh Poovazhagi, Varadarajan Kanthimathi, Sekar Balamurugan, Kandasamy Bodhini, Dhanasekaran Yadav, Jaivinder Jain, Vandana Khadgawat, Rajesh Sikdar, Mahuya Bhavatharini, Ayurchelvan Das, Ashok Kumar Kaur, Tanvir Mohan, Viswanathan Radha, Venkatesan Producer: 20150408 In: Annals of human genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)