Barely Significant
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Genotype-Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants.

Genes (Basel) · 2023 · PMC10671142 · PMID 38002959

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moderately significantno p-value reported
However, these differences were only moderately significant, while international scientists who conducted similar studies on significantly larger samples of FD patients identified significant differences both in the accumulated substrate levels and in the age of diagnosis between patient groups with classical FD and atypical FD, and could be caused by the different genome variants [ 42 , 43 ].

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