The Case of “Missing Causal Genes” and the Practice of Medicine
Author:
Affiliation:
1. From the Department of Medicine, Center for Cardiovascular Genetics, Brown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center, Texas Heart Institute, Houston.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine,Physiology
Link
https://www.ahajournals.org/doi/pdf/10.1161/CIRCRESAHA.116.308830
Reference22 articles.
1. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
2. HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
3. Genetics of Sudden Cardiac Death
4. Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics
5. Estimating the human mutation rate using autozygosity in a founder population
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