Cellular and Molecular Alterations Underlying Abnormal Bone Growth in X-Linked Hypophosphatemia

X-linked hypophosphatemia (XLH), the most common form of hereditary hypophosphatemic rickets, is caused by inactivating mutations of the phosphate-regulating endopeptidase gene (PHEX). XLH is mainly characterized by short stature, bone deformities and rickets, while in hypophosphatemia, normal or lo...

Descripción completa

Detalles Bibliográficos
Autores principales: Fuente, Rocío, García-Bengoa, María, Fernández-Iglesias, Ángela, Gil-Peña, Helena, Santos, Fernando, López, José Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778463/
https://www.ncbi.nlm.nih.gov/pubmed/35055123
http://dx.doi.org/10.3390/ijms23020934

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778463/
https://www.ncbi.nlm.nih.gov/pubmed/35055123
http://dx.doi.org/10.3390/ijms23020934

Ejemplares similares