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Phenotypic Diversity in Pediatric Congenital Myasthenic Syndrome: Insights from CHRNE and DPAGT1 Variants — Europe PMC PMID:42347111

Source
Europe PMC (en)
Original
https://europepmc.org/article/MED/42347111
DOI
10.3390/neurolint18060102
License (as archived)
solo-consultazione
Archived
2026-11-01T07:51:15.609Z
SHA-256 of the archived text
7c1d0c2225c7b3c5b5226096b68a64d469b49186d5dec389c445a28832f803ac
Stable URL of this page
https://metraipolis.com/documento/dc_fdcf69075bc2

How to cite

Phenotypic Diversity in Pediatric Congenital Myasthenic Syndrome: Insights from CHRNE and DPAGT1 Variants — Europe PMC PMID:42347111 — Europe PMC (en), https://europepmc.org/article/MED/42347111 (solo-consultazione); archived copy: https://metraipolis.com/documento/dc_fdcf69075bc2 (Metraipolis archive dc_fdcf69075bc2, sha256 7c1d0c2225c7b3c5b5226096b68a64d469b49186d5dec389c445a28832f803ac)
BibTeX
@misc{dcfdcf69075bc2,
  title = {Phenotypic Diversity in Pediatric Congenital Myasthenic Syndrome: Insights from CHRNE and DPAGT1 Variants — Europe PMC PMID:42347111},
  howpublished = {Europe PMC (en)},
  url = {https://europepmc.org/article/MED/42347111},
  note = {License solo-consultazione; archived copy https://metraipolis.com/documento/dc_fdcf69075bc2; sha256 7c1d0c2225c7b3c5b5226096b68a64d469b49186d5dec389c445a28832f803ac},
  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/42347111. Agents can read the archived copy with the MCP tool read_document.