Publication | Closed Access
Mutational analysis of patients with FGF23-related hypophosphatemic rickets
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Citations
32
References
2012
Year
XLHR is by far the most prevalent cause of FGF23-related hypophosphatemic rickets. We propose that analysis of PHEX mRNA from peripheral blood would be appropriate for the first screening step in determining the etiology of FGF23-related hypophosphatemic rickets.
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