Annals of Indian Academy of Neurology
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1KCNQ1mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1
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
American Journal of Medical Genetics Part A.2016;170(6)1510
[DOI]
2“Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports”
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BMC Medical Genetics.2017;18(1)1510
[DOI]
3Cerebral Seizures in an Adolescent with Jervell and Lange-Nielsen Syndrome: It May Not Be Epilepsy
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4“Who” Can be Found in and beyond of an Electrocardiographic Strip
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Pacing and Clinical Electrophysiology.2014;37(3)265
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5Variant frequencies of KCNQ1 , KCNH2 , and SCN5A in a Chinese inherited arrhythmia cohort and other disease cohorts undergoing genetic testing
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Annals of Human Genetics.2020;84(2)161
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6Inherited arrhythmia syndromes leading to sudden cardiac death in the young: A global update and an Indian perspective
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Indian Heart Journal.2014;66(2)S49
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7Jervell and Lange–Nielsen Syndrome: Homozygous Missense Mutation of KCNQ1 in a Turkish Family
Ozlem Bostan,Sehime G. Temel,Hakan Cangül,Caroline N. S. Archer,Ergun Çil
Pediatric Cardiology.2013;34(8)2063
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8Channelopathies - Emerging Trends in The Management of Inherited Arrhythmias
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Indian Pacing and Electrophysiology Journal.2015;15(1)43
[DOI]
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