Inactivating mutations of the gene coding for phosphate-regulating endopeptidase homolog X-linked (PHEX) cause X-linked hypophosphatemia (XLH). A nove
X-linked hypophosphatemia (XLH) is a rare X-linked dominant inherited disorder caused by loss-of-fun...
Twenty-five years ago, a pathogenic variant of the phosphate-regulating endopeptidase homolog X-link...
X-linked hypophosphatemia (XLH) is a rare inheritable disorder of phosphate handling due to loss of ...
X-linked hypophosphatemia (XLH) is caused by mutations in PHEX. Several other genetic forms of hypop...
Introduction and Aim X-linked hypophosphatemic rickets, inherited in a dominant manner, is the most ...
Loss of function mutations in the PHEX gene could determine X-linked dominant hypophosphatemia. This...
X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function mutations in...
Copyright © 2015 Tetsuya Kawahara et al. This is an open access article distributed under the Creati...
Phosphate regulating gene with homologies to endopeptidases on the X-chromosome (PHEX) is a common c...
X-linked hypophosphatemic rickets (XLH) is a dominant inherited disorder characterized by renal phos...
Phosphate regulating gene with homologies to endopeptidases on the X-chromosome (PHEX) is a common c...
Hypophosphatemic rickets (HR) is a heterogeneous genetic phosphate wasting disorder. The disease is ...
Hypophosphatemic rickets is commonly an X-linked dominant disorder (XLH or HYP) associated with a re...
Objectives Lower limb deformities in children need careful orthopedic evaluation to distinguish phys...
Background: X-linked hypophosphatemia (XLH) is an inherited disease of phosphate metabolism in which...
X-linked hypophosphatemia (XLH) is a rare X-linked dominant inherited disorder caused by loss-of-fun...
Twenty-five years ago, a pathogenic variant of the phosphate-regulating endopeptidase homolog X-link...
X-linked hypophosphatemia (XLH) is a rare inheritable disorder of phosphate handling due to loss of ...
X-linked hypophosphatemia (XLH) is caused by mutations in PHEX. Several other genetic forms of hypop...
Introduction and Aim X-linked hypophosphatemic rickets, inherited in a dominant manner, is the most ...
Loss of function mutations in the PHEX gene could determine X-linked dominant hypophosphatemia. This...
X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function mutations in...
Copyright © 2015 Tetsuya Kawahara et al. This is an open access article distributed under the Creati...
Phosphate regulating gene with homologies to endopeptidases on the X-chromosome (PHEX) is a common c...
X-linked hypophosphatemic rickets (XLH) is a dominant inherited disorder characterized by renal phos...
Phosphate regulating gene with homologies to endopeptidases on the X-chromosome (PHEX) is a common c...
Hypophosphatemic rickets (HR) is a heterogeneous genetic phosphate wasting disorder. The disease is ...
Hypophosphatemic rickets is commonly an X-linked dominant disorder (XLH or HYP) associated with a re...
Objectives Lower limb deformities in children need careful orthopedic evaluation to distinguish phys...
Background: X-linked hypophosphatemia (XLH) is an inherited disease of phosphate metabolism in which...
X-linked hypophosphatemia (XLH) is a rare X-linked dominant inherited disorder caused by loss-of-fun...
Twenty-five years ago, a pathogenic variant of the phosphate-regulating endopeptidase homolog X-link...
X-linked hypophosphatemia (XLH) is a rare inheritable disorder of phosphate handling due to loss of ...
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