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Published in 2021 at "Internal medicine"
DOI: 10.2169/internalmedicine.8137-21
Abstract: Muscle phosphorylase b kinase (PHK) deficiency is a rare mild metabolic disorder caused by mutations of the PHKA1 gene encoding the αM subunit of PHK. A 16-year-old boy experienced myalgia during the maximal multistage 20-m…
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Keywords:
multistage shuttle;
maximal multistage;
muscle;
test ... See more keywords