PHEX Gene Mutation in a Patient with X-Linked Hypophosphatemic Rickets in a Developing Country. [electronic resource]

By: Contributor(s): Publication details: The application of clinical genetics 2020Description: 57-62 p. digitalISSN:
  • 1178-704X
Online resources: In: The application of clinical genetics vol. 13
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Publication Type: Case Reports; Journal Article

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