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A Novel PHEX Gene Mutation in a Patient with Sporadic Hypophosphatemic Rickets
Phosphate regulating gene with homologies to endopeptidases on the X-chromosome (PHEX) is a common cause of X-linked hypophosphatemic (XLH) rickets. Diverse PHEX gene mutations have been reported; however, gene mutations in sporadic rickets are less common than in XLH rickets. Herein, we describe a...
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| Glavni autori: | , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Korean Endocrine Society
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4091495/ https://ncbi.nlm.nih.gov/pubmed/25031893 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3803/EnM.2014.29.2.195 |
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