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Assessing the Functional Significance of Novel and Rare Variants of the SLC26A4 Gene Found in Patients with Hearing Loss by Minigene Assay — Europe PMC PMID:41226768

Source: Europe PMC (en)
Original: https://europepmc.org/article/MED/41226768
DOI: 10.3390/ijms262110732
License (as archived): solo-consultazione
Archived: 2026-11-08T19:42:08.138Z
SHA-256 of the archived text: a4daef137c846bda5b3dfbcc017e5b369bc8045de3b24d7fcb9631c82ac83b09
Stable URL of this page: https://metraipolis.com/documento/dc_4967503ea5aa

How to cite

Assessing the Functional Significance of Novel and Rare Variants of the SLC26A4 Gene Found in Patients with Hearing Loss by Minigene Assay — Europe PMC PMID:41226768 — Europe PMC (en), https://europepmc.org/article/MED/41226768 (solo-consultazione); archived copy: https://metraipolis.com/documento/dc_4967503ea5aa (Metraipolis archive dc_4967503ea5aa, sha256 a4daef137c846bda5b3dfbcc017e5b369bc8045de3b24d7fcb9631c82ac83b09)

BibTeX

@misc{dc4967503ea5aa,
  title = {Assessing the Functional Significance of Novel and Rare Variants of the SLC26A4 Gene Found in Patients with Hearing Loss by Minigene Assay — Europe PMC PMID:41226768},
  howpublished = {Europe PMC (en)},
  url = {https://europepmc.org/article/MED/41226768},
  note = {License solo-consultazione; archived copy https://metraipolis.com/documento/dc_4967503ea5aa; sha256 a4daef137c846bda5b3dfbcc017e5b369bc8045de3b24d7fcb9631c82ac83b09},
  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/41226768. Agents can read the archived copy with the MCP tool read_document.