S-EPMC11614792 - Newly identified intronic and known pathogenic point mutations in <i>SLC34A3/NPT2c</i> cause hereditary hypophosphatemic rickets with hypercalciuria. - OmicsDI

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Newly identified intronic and known pathogenic point mutations in <i>SLC34A3/NPT2c</i> cause hereditary hypophosphatemic rickets with hypercalciuria.

ABSTRACT:

SUBMITTER: Sun Y

PROVIDER: S-EPMC11614792 | biostudies-literature | 2025 Mar

REPOSITORIES: biostudies-literature