Associated Papers
Phosphate homeostasis disorders.
Christov M et al.
Best Practice & Research. Clinical Endocrinology & Metabolism, 2018
Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosis.
Rajagopal A et al.
The Journal of Clinical Endocrinology and Metabolism, 2014
NPT2a gene variation in calcium nephrolithiasis with renal phosphate leak.
Lapointe JY et al.
Kidney International, 2006
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