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Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in SOST Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature — Europe PMC PMID:40943101

Source: Europe PMC (en)
Original: https://europepmc.org/article/MED/40943101
DOI: 10.3390/ijms26178175
License (as archived): solo-consultazione
Archived: 2026-11-10T10:58:48.069Z
SHA-256 of the archived text: bcf8c3b195b439af1468ff1a7deaea172eddf7f877bbf85531f8dff34ce67ee2
Stable URL of this page: https://metraipolis.com/documento/dc_53d2014f2913

How to cite

Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in SOST Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature — Europe PMC PMID:40943101 — Europe PMC (en), https://europepmc.org/article/MED/40943101 (solo-consultazione); archived copy: https://metraipolis.com/documento/dc_53d2014f2913 (Metraipolis archive dc_53d2014f2913, sha256 bcf8c3b195b439af1468ff1a7deaea172eddf7f877bbf85531f8dff34ce67ee2)

BibTeX

@misc{dc53d2014f2913,
  title = {Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in SOST Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature — Europe PMC PMID:40943101},
  howpublished = {Europe PMC (en)},
  url = {https://europepmc.org/article/MED/40943101},
  note = {License solo-consultazione; archived copy https://metraipolis.com/documento/dc_53d2014f2913; sha256 bcf8c3b195b439af1468ff1a7deaea172eddf7f877bbf85531f8dff34ce67ee2},
  year = {2026}
}

Archived text

The text is not reproduced here: the archive holds it as solo-consultazione (consultation only, no republication). Read it at the original source: https://europepmc.org/article/MED/40943101. Agents can read the archived copy with the MCP tool read_document.