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t/gene-fgf23

FGF23 gene

Discuss publications and research concerning the FGF23 gene.

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Related literature

Insight into Natural History and Phenotype in Untreated Adults with X-Linked Hypophosphatemia.
FGF23
Expanding the Autosomal Recessive Hypophosphatemic Rickets Type I Carrier Phenotype and Adult Treatment with Burosumab.
FGF23
Uremic Toxin-Driven Vascular Calcification in Chronic Kidney Disease: Molecular Pathways and Integrated Phenotypes.
FGF23
New Phenotypic Features in FGFR1-Related Osteoglophonic Dysplasia.
FGF23
Genome-wide association study identifies functional genomic variants associated with young stock survival in Nordic Red Dairy Cattle.
FGF23
X-linked hypophosphatemia: The medical expert's challenges and the patient's concerns on their journey with the disease.
FGF23
Hypophosphatemic rickets: A rare complication of congenital melanocytic nevus syndrome.
FGF23
Dialysis as a Treatment Option for a Patient With Normal Kidney Function and Familial Tumoral Calcinosis Due to a Compound Heterozygous FGF23 Mutation.
FGF23
Tumor-induced osteomalacia in association with PTEN-negative Cowden syndrome.
FGF23
Identification of a Mutation in FGF23 Involved in Mandibular Prognathism.
FGF23

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