Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype.

This difference between the homozygous and control cells was highly significant (p values = 5.6 × 10 −4 and 1.7 × 10 −7 for 1401 and 1402, respectively; Wilcoxon test).

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