Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death-Reference-Cited by-同舟云学术

Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death

Published:2015-07-19 Issue:1 Volume:9 Page:
ISSN:1479-7364
Container-title:Human Genomics
language:en
Short-container-title:Hum Genomics

Author:

Li Mindy H.,Abrudan Jenica L.,Dulik Matthew C.,Sasson Ariella,Brunton Joshua,Jayaraman Vijayakumar,Dugan Noreen,Haley Danielle,Rajagopalan Ramakrishnan,Biswas Sawona,Sarmady Mahdi,DeChene Elizabeth T.,Deardorff Matthew A.,Wilkens Alisha,Noon Sarah E.,Scarano Maria I.,Santani Avni B.,White Peter S.,Pennington Jeffrey,Conlin Laura K.,Spinner Nancy B.,Krantz Ian D.,Vetter Victoria L.

Funder

National Human Genome Research Institute

National Institute of General Medical Sciences

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1186/s40246-015-0038-y.pdf

Reference23 articles.

1. Jamal SM, Yu J, Chong JX, Dent KM, Conta JH, Tabor HK, Bamshad MJ. Practices and Policies of Clinical Exome Sequencing Providers: Analysis and Implications. Am J Med Genet A. 2013;161A:n/a-n/a.

2. Interpreting Secondary Cardiac Disease Variants in an Exome Cohort. Circ Cardiovasc Genet. 2013;6:337–46.