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Ross T Murphy

Showing results (41-50 of 44) with videos related to

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Molecular Genetics and Metabolism|October 22, 2003
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosisBhagyalaxmi Mohapatra, Shinawe Jimenez, Jiuann Huey Lin, et al.
Open Heart|June 26, 2021
Interhospital and interindividual variability in secondary prevention: a comparison of outpatients with a history of chronic coronary syndrome versus outpatients with a history of acute coronary syndrome (the iASPIRE Study)James Mg Curneen, Conor Judge, Bryan Traynor, et al.
Journal of the American College of Cardiology|December 10, 2003
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compactionMatteo Vatta, Bhagyalaxmi Mohapatra, Shinawe Jimenez, et al.
Human Molecular Genetics|January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutationsEnkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
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Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Molecular Genetics and Metabolism|October 22, 2003
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosisBhagyalaxmi Mohapatra, Shinawe Jimenez, Jiuann Huey Lin, et al.
Open Heart|June 26, 2021
Interhospital and interindividual variability in secondary prevention: a comparison of outpatients with a history of chronic coronary syndrome versus outpatients with a history of acute coronary syndrome (the iASPIRE Study)James Mg Curneen, Conor Judge, Bryan Traynor, et al.
Journal of the American College of Cardiology|December 10, 2003
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compactionMatteo Vatta, Bhagyalaxmi Mohapatra, Shinawe Jimenez, et al.
Human Molecular Genetics|January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutationsEnkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
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