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Heimler Syndrome Caused by Novel PEX6 Variants: Clinical and Genetic Characterization in a Saudi Cohort — Europe PMC PMID:42074478

Source: Europe PMC (en)
Original: https://europepmc.org/article/MED/42074478
DOI: 10.3390/genes17040360
License (as archived): solo-consultazione
Archived: 2026-11-03T23:38:12.731Z
SHA-256 of the archived text: b24992ae4ac61cbc41f66446c71cbf0de991815102bf43234f45c59d55382464
Stable URL of this page: https://metraipolis.com/documento/dc_abebcc3ea8db

How to cite

Heimler Syndrome Caused by Novel PEX6 Variants: Clinical and Genetic Characterization in a Saudi Cohort — Europe PMC PMID:42074478 — Europe PMC (en), https://europepmc.org/article/MED/42074478 (solo-consultazione); archived copy: https://metraipolis.com/documento/dc_abebcc3ea8db (Metraipolis archive dc_abebcc3ea8db, sha256 b24992ae4ac61cbc41f66446c71cbf0de991815102bf43234f45c59d55382464)

BibTeX

@misc{dcabebcc3ea8db,
  title = {Heimler Syndrome Caused by Novel PEX6 Variants: Clinical and Genetic Characterization in a Saudi Cohort — Europe PMC PMID:42074478},
  howpublished = {Europe PMC (en)},
  url = {https://europepmc.org/article/MED/42074478},
  note = {License solo-consultazione; archived copy https://metraipolis.com/documento/dc_abebcc3ea8db; sha256 b24992ae4ac61cbc41f66446c71cbf0de991815102bf43234f45c59d55382464},
  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/42074478. Agents can read the archived copy with the MCP tool read_document.