Barely Significant
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Genetics of tuberous sclerosis complex: implications for clinical practice.

Appl Clin Genet · 2017 · PMC5189696 · PMID 28053551

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may be significantno p-value reported
20 , 21 However, there may be significant overlap in disease severity between TSC1 and TSC2 patients, and many individuals with TSC1 mutations have severe multiorgan system involvement.

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