A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation☆☆☆★
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☆ Supported by NIH grant 1RO1HL58626 (Dr Hershberger).
☆☆ Reprint requests: Ray E. Hershberger, MD, Department of Medicine/Cardiology, UHN-62, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd, Portland, OR 97201.
★ E-mail: hershber@ohsu.edu, or www.fdc.to
PII: S0002-8703(02)00234-X
doi:10.1067/mhj.2002.126737
© 2002 Mosby, Inc. All rights reserved.
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