KCNQ1mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1-Reference-Cited by-同舟云学术

KCNQ1mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1

Published:2016-04-04 Issue:6 Volume:170 Page:1510-1519
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Vyas Bijal¹,Puri Ratna D.¹,Namboodiri Narayanan²,Nair Mohan³,Sharma Deepak⁴,Movva Sireesha¹,Saxena Renu¹,Bohora Shomu⁵,Aggarwal Neeraj⁶,Vora Amit⁷,Kumar Jatinder⁴,Singh Tarandeep⁸,Verma Ishwar C.¹

Affiliation:

1. Centre of Medical Genetics; Sir Ganga Ram Hospital; Delhi India

2. Department of Cardiology; Sree Chitra Institute for Medical Sciences & Technology; Kerala India

3. Department of Cardiology; Holy Family Hospital; Delhi India

4. Department of Biotechnology; Indian Institute of Technology Roorkee; Roorkee Uttarakhand India

5. Department of Cardiology; Baroda Heart Institute & Research Centre; Gujarat India

6. Department of Paediatric Cardiology; Sir Ganga Ram Hospital; Delhi India

7. Department of Cardiology; Glenmark Cardiac Centre; Mumbai Maharashtra India

8. Department of Cardiology; U N Mehta Institute of Cardiology & Research Centre; Gujarat India

Funder

Research Development Program, Sir Ganga Ram Hospital

Department of Health Research (DHR)/Indian Council of Medical Research (ICMR)

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference43 articles.

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3. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome;Bhuiyan;Prog Biophys Mol Biol,2008

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