Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation is a research paper published in Human Molecular Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 29 times.
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National Heart, Lung and Blood Institute of the National Institutes of Health
Grant: R01HL142903
National Institutes of Health
Grant: 1R01HL142903-01A1
Ryanodine Receptor Defects in Cardiomyopathy Caused by Lamin A/C Gene Mutations
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Sustainable Development Goals