Mutation-Specific Calcium Dysregulation in Hypertrophic Cardiomyopathy
As the genetic causes of Hypertrophic Cardiomyopathy (HCM) have become widely recognized, considerable lag in the development of targeted therapeutics has limited interventions to symptom palliation. This is in part due to an oft-noted finding that similar point mutations within myofilament proteins...
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| Language: | en_US |
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The University of Arizona.
2018
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| Online Access: | http://hdl.handle.net/10150/626641 http://arizona.openrepository.com/arizona/handle/10150/626641 |