Barely Significant
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Caveolin-3 deficiency associated with the dystrophy P104L mutation impairs skeletal muscle mitochondrial form and function.

J Cachexia Sarcopenia Muscle · 2020 · PMC7296273 · PMID 32090499

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may be significantno p-value reported
protein synthesis) that may be significant in the pathology of LGMD1C.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.