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Paper Details

Severe vascular calcification and tumoral calcinosis in a family with hyperphosphatemia: a fibroblast growth factor 23 mutation identified by exome sequencing.
Nephrol Dial Transplant
21
2014
C, FGF23, FGF23 homologue, N, N-terminal FGF23, Q67K, Tumoral calcinosis, autosomal recessive disorder, fibroblast, fibroblast growth factor 23, human, hyperphosphatemia, metabolic anomaly, null (deletion) allele, plasma C-terminal FGF23, tumoral calcinosis, vascular calcification, vascular cells
Author NameAffiliation
Mark D AdamsJ. Craig Venter Institute
Sharon G AdlerLos Angeles Biomedical Research Institute at Harbor-university of california los angeles Medical Center
Sudha K IyengarCase Western Reserve University School of Medicine
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Datasets

Release 1.2