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Article

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

1 Nov 2000

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 11062477
DOI: 10.1038/81664

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Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23PMID 11062477Read ↗

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Hypophosphatemic Rickets with R179W Mutation in FGFR23 Gene - A Rare But Treatable Cause of Refractory Rickets.Semantic proximity Read ↗

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Genetic and clinical profile of patients with hypophosphatemic ricketsSemantic proximity Read ↗

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An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation.Semantic proximity Read ↗

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