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Published in 2022 at "Genes"
DOI: 10.3390/genes13122415
Abstract: X-linked hypophosphatemia (XLH) is the most common hereditary form of rickets and deficiency of renal tubular phosphate transport in humans. XLH is caused by the inactivation of mutations within the phosphate-regulating endopeptidase homolog X-linked (PHEX)…
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Keywords:
phosphate;
muscle;
impact linked;
hypophosphatemia muscle ... See more keywords