Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy von Parks, Sharie B., PhD, Kushner, Jessica D., MS, CGC, Nauman, Deirdre, BSN, Burgess, Donna, BSN, Ludwigsen, Susan, MA, Peterson, Amanda, BS, Li, Duanxiang, MD, Jakobs, Petra, PhD, Litt, Michael, PhD, Porter, Charles B., MD, FACC, Rahko, Peter S., MD, FACC, Hershberger, Ray E., MD, FACC

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Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure von Li, Duanxiang, Parks, Sharie B., Kushner, Jessica D., Nauman, Deirdre, Burgess, Donna, Ludwigsen, Susan, Partain, Julie, Nixon, Randal R., Allen, Charles N., Irwin, Robert P., Jakobs, Petra M., Litt, Michael, Hershberger, Ray E.

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Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy von Hershberger, Ray E, Pinto, Jose Renato, Parks, Sharie B, Kushner, Jessica D, Li, Duanxiang, Ludwigsen, Susan, Cowan, Jason, Morales, Ana, Parvatiyar, Michelle S, Potter, James D

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Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy von Hershberger, Ray E., Parks, Sharie B., Kushner, Jessica D., Li, Duanxiang, Ludwigsen, Susan, Jakobs, Petra, Nauman, Deirdre, Burgess, Donna, Partain, Julie, Litt, Michael

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Clinical Characteristics of 304 Kindreds Evaluated for Familial Dilated Cardiomyopathy von Kushner, Jessica D., Nauman, Deirdre, Burgess, Donna, Ludwigsen, Susan, Parks, Sharie B., Pantely, George, Burkett, Emily, Hershberger, Ray E.

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Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes von PARKS, Sharie B, POPOVICH, Bradley W, PRESS, Richard D

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Diagnostic Molecular Pathology

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