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Supplementary Material for: Composite Phenotype: Recurrent Nephrolithiasis and Chronic Kidney Disease in an Adult with Biallelic SLC34A3 and Monoallelic SLC3A1 Pathogenic Variants: Who is ‘The Culprit’?

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Figshare2026-03-18 更新2026-04-28 收录
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https://figshare.com/articles/dataset/Supplementary_Material_for_Composite_Phenotype_Recurrent_Nephrolithiasis_and_Chronic_Kidney_Disease_in_an_Adult_with_Biallelic_SLC34A3_and_Monoallelic_SLC3A1_Pathogenic_Variants_Who_is_The_Culprit_/31798708
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Kidney stones are common and can arise from many etiologies including genetic and environmental. Biallelic pathogenic variants in the solute carrier family 34-member 3 (SLC34A3) gene cause Hereditary Hypophosphatemic Rickets with Hypercalciuria (HHRH), while both monallaelic and biallelic pathogenic variants in SLC3A1 cause cystinuria. Here, we report the clinical phenotype of a patient with concomitant biallelic and monoallelic pathogenic variants in SLC34A3 and SLC3A1 respectively.
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2026-03-18
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