Hyperphosphatemia With Normal Kidney Function Associated With Genetic Variants of GALNT3
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference9 articles.
1. Phenotypic and genotypic characterization and treatment of a cohort with familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome;Ramnitz;J Bone Miner Res,2016
2. Hyperphosphatemic tumoral calcinosis: pathogenesis, clinical presentation, and challenges in management;Boyce;Front Endocrinol (Lausanne),2020
3. Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature;Rafaelsen;BMC Genet,2014
4. A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features;Dumitrescu;Osteoporos Int,2009
5. Novel mutations in GALNT3 causing hyperphosphatemic familial tumoral calcinosis;Yancovitch;J Bone Miner Metab,2011
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