Genotype‐phenotype correlation of K ATP channel gene defects causing permanent neonatal diabetes in Indian patients-Reference-Cited by-同舟云学术

Genotype‐phenotype correlation of K ATP channel gene defects causing permanent neonatal diabetes in Indian patients

Published:2020-09-15 Issue:1 Volume:22 Page:82-92
ISSN:1399-543X
Container-title:Pediatric Diabetes
language:en
Short-container-title:Pediatr Diabetes

Author:

Gopi Sundaramoorthy¹,Kavitha Babu¹,Kanthimathi Sekar¹,Kannan Alagarsamy²,Kumar Rakesh³^ORCID,Joshi Rajesh⁴,Kanodia Swati⁵,Arya Archana Dayal⁶,Pendsey Sanket⁷,Pendsey Sharad⁷,Raghupathy Palany⁸,Mohan Viswanathan²⁹^ORCID,Radha Venkatesan¹^ORCID

Affiliation:

1. Department of Molecular Genetics, Madras Diabetes Research Foundation ICMR Advanced Centre for Genomics of Type 2 Diabetes, Affiliated to University of Madras Chennai India

2. Dr. Mohan's Diabetes Specialities Centre, WHO Collaborating Centre for Non‐Communicable Diseases Prevention & Control, IDF Centre of Education Chennai India

3. Advanced Paediatrics Centre, Post‐Graduate Institute of Medical Education and Research (PGIMER) Chandigarh India

4. Division of Paediatric Endocrinology B.J. Wadia Hospital for Children Mumbai India

5. BLK Super Speciality Hospital New Delhi India

6. Institute of Child Health Sir Ganga Ram Hospital Marg New Delhi India

7. Diabetes Clinic & Research Centre Nagpur India

8. Department of Paediatrics Sagar Hospitals Bangalore India

9. Department of Diabetology Madras Diabetes Research Foundation Chennai India

Funder

Indian Council of Medical Research

Publisher

Wiley

Subject