KCNQ1 mutations associated with Jervell and Lange–Nielsen syndrome and autosomal recessive Romano–Ward syndrome in India—expanding the spectrum of long QT syndrome type 1期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

KCNQ1 mutations associated with Jervell and Lange–Nielsen syndrome and autosomal recessive Romano–Ward syndrome in India—expanding the spectrum of long QT syndrome type 1

Authors:	Bijal Vyas Ratna D. Puri Narayanan Namboodiri Mohan Nair Deepak Sharma Sireesha Movva Renu Saxena Shomu Bohora Neeraj Aggarwal Amit Vora Jatinder Kumar Tarandeep Singh Ishwar C. Verma

Affiliation:	1. Centre of Medical Genetics, Sir Ganga Ram Hospital, Delhi, India;2. Correspondence to:;3. Dr. Ratna D. Puri, Centre of Medical Genetics, Sir Ganga Ram Hospital, Rajinder Nagar, Delhi 110060, India.;4. Department of Cardiology, Sree Chitra Institute for Medical Sciences & Technology, Kerala, India;5. Department of Cardiology, Holy Family Hospital, Delhi, India;6. Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, India;7. Department of Cardiology, Baroda Heart Institute & Research Centre, Gujarat, India;8. Department of Paediatric Cardiology, Sir Ganga Ram Hospital, Delhi, India;9. Department of Cardiology, Glenmark Cardiac Centre, Mumbai, Maharashtra, India;10. Department of Cardiology, U N Mehta Institute of Cardiology & Research Centre, Gujarat, India

Abstract:

Keywords:	biallelic deafness genetics Indian KCNQ1 long QT syndrome recessive sequencing homozygous