docx, 1.59 MB
docx, 1.59 MB
docx, 1.6 MB
docx, 1.6 MB
pdf, 462.38 KB
pdf, 462.38 KB
pdf, 326.5 KB
pdf, 326.5 KB
This activity explains how hypertrophic cardiomyopathy (HCM) is caused by genetic mutations, and the impacts of these mutations on protein synthesis. Students learn how the structure and function of the heart, and the use of ATP by the heart, are affected by HCM. To see more like this, visit: https://www.youtube.com/user/OxfordSparks/videos © 2014 University of Oxford
Tes classic free licence

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