Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis - Concepedia

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Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis

DOI Full Paper Access

58

Citations

30

References

2013

Year

Blanka Stibůrková, Ivan Šebesta, Kimiyoshi Ichida, Makiko Nakamura, Helena Hůlková, Vladimír Krylov, Lenka Kryspinova, Helena Jahnová

European Journal of Human Genetics

Allelic VariantUrologyRenal FunctionPrevalent MutationMedicineGeneticsIga GlomerulonephritisRenal PathologyRenal HypouricemiaPathologyMolecular GeneticsRenal PathophysiologyChronic Kidney DiseaseNephrologyKidney ResearchNovel Allelic Variants

References

	Year	Citations

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