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Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophy — Europe PMC PMID:40861057

Source: Europe PMC (en)
Original: https://europepmc.org/article/MED/40861057
DOI: 10.3389/fped.2025.1650645
License (as archived): solo-consultazione
Archived: 2026-11-10T17:44:43.070Z
SHA-256 of the archived text: 0cb8912fa4478a611a15b990d301c3633932f89e4cecb67361384d4c13386bde
Stable URL of this page: https://metraipolis.com/documento/dc_d20076ce4e85

How to cite

Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophy — Europe PMC PMID:40861057 — Europe PMC (en), https://europepmc.org/article/MED/40861057 (solo-consultazione); archived copy: https://metraipolis.com/documento/dc_d20076ce4e85 (Metraipolis archive dc_d20076ce4e85, sha256 0cb8912fa4478a611a15b990d301c3633932f89e4cecb67361384d4c13386bde)

BibTeX

@misc{dcd20076ce4e85,
  title = {Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophy — Europe PMC PMID:40861057},
  howpublished = {Europe PMC (en)},
  url = {https://europepmc.org/article/MED/40861057},
  note = {License solo-consultazione; archived copy https://metraipolis.com/documento/dc_d20076ce4e85; sha256 0cb8912fa4478a611a15b990d301c3633932f89e4cecb67361384d4c13386bde},
  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/40861057. Agents can read the archived copy with the MCP tool read_document.