Impact of X-Linked Hypophosphatemia on Muscle Symptoms.
FGF23
X-linked hypophosphatemia
muscle weakness
skeletal muscle
skeletal muscle dysfunction
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
19 12 2022
19 12 2022
Historique:
received:
02
11
2022
revised:
08
12
2022
accepted:
15
12
2022
entrez:
23
12
2022
pubmed:
24
12
2022
medline:
27
12
2022
Statut:
epublish
Résumé
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 (
Identifiants
pubmed: 36553684
pii: genes13122415
doi: 10.3390/genes13122415
pmc: PMC9778127
pii:
doi:
Substances chimiques
Phosphates
0
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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