Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease.

Kidney Int Rep · 2021 · PMC8589729 · PMID 34805638

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may be significantno p-value reported

All 4 SLC34A3 patients were identified in the DDN cohort; 1 was homozygous, 2 alleles were novel, and in 2 families 3 alleles that may be significant were detected ( Tables 1 and 2 ; Figure 2 a, b 47 ).

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