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Mitochondrial HMG-CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant — Europe PMC PMID:41383544

Source: Europe PMC (en)
Original: https://europepmc.org/article/MED/41383544
DOI: 10.1002/ccr3.71622
License (as archived): solo-consultazione
Archived: 2026-11-07T19:12:51.534Z
SHA-256 of the archived text: c07f60279eff028dbd205e77ea45235361abf7ff2be969895150b131d7f2c918
Stable URL of this page: https://metraipolis.com/documento/dc_320814c70125

How to cite

Mitochondrial HMG-CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant — Europe PMC PMID:41383544 — Europe PMC (en), https://europepmc.org/article/MED/41383544 (solo-consultazione); archived copy: https://metraipolis.com/documento/dc_320814c70125 (Metraipolis archive dc_320814c70125, sha256 c07f60279eff028dbd205e77ea45235361abf7ff2be969895150b131d7f2c918)

BibTeX

@misc{dc320814c70125,
  title = {Mitochondrial HMG-CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant — Europe PMC PMID:41383544},
  howpublished = {Europe PMC (en)},
  url = {https://europepmc.org/article/MED/41383544},
  note = {License solo-consultazione; archived copy https://metraipolis.com/documento/dc_320814c70125; sha256 c07f60279eff028dbd205e77ea45235361abf7ff2be969895150b131d7f2c918},
  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/41383544. Agents can read the archived copy with the MCP tool read_document.