Associated Papers
Global genetic prevalence estimates of primary hyperoxaluria are greater than previously reported.
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Clinical Kidney Journal, 2025
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Supplement: sfaf194_Supplemental_File.docx
A novel nonsense variant of the AGXT identified in a Chinese family: special variant research in the Chinese reference genome.
Xu CB et al.
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Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria.
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Journal of the American Society of Nephrology : Jasn, 2015
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