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A Loss-of-Function Mutation in NaPi-IIa and Renal Fanconi's Syndrome - New England Journal of Medicine (subscription) PDF Print
New England Journal of Medicine (subscription)Genetic analysis revealed a homozygous in-frame duplication of 21 bp in SLC34A1, which encodes the renal sodium–inorganic phosphate cotransporter NaPi-IIa,

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