Impact of X-Linked Hypophosphatemia on Muscle Symptoms

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) gene and follows an X-dominant transmissio...

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Detalles Bibliográficos
Autores principales: Romagnoli, Cecilia, Iantomasi, Teresa, Brandi, Maria Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778127/
https://www.ncbi.nlm.nih.gov/pubmed/36553684
http://dx.doi.org/10.3390/genes13122415

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778127/
https://www.ncbi.nlm.nih.gov/pubmed/36553684
http://dx.doi.org/10.3390/genes13122415

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