Return of Genetic Results in the Familial Dilated Cardiomyopathy Research Project
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-012-9532-8
Reference40 articles.
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2. Bookman, E. B., Langehorne, A. A., Eckfeldt, J. H., Glass, K. C., Jarvik, G. P., Klag, M., et al. (2006). Reporting genetic results in research studies: summary and recommendations of an NHLBI working group. American Journal of Medical Genetics. Part A, 140(10), 1033–1040.
3. Burkett, E. L., & Hershberger, R. E. (2005). Clinical and genetic issues in familial dilated cardiomyopathy. Journal of the American College of Cardiology, 45(7), 969–981.
4. Caleshu, C., Day, S., Rehm, H. L., & Baxter, S. (2010). Use and interpretation of genetic tests in cardiovascular genetics. Heart, 96(20), 1669–1675.
5. Cheng, J., Morales, A., Siegfried, J. D., Li, D., Norton, N., Song, J., et al. (2010). SCN5A rare variants in familial dilated cardiomyopathy decrease peak sodium current depending on the common polymorphism H558R and splice variant Q1077del. Clin Trans Sci, 3, 287–294.
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