APA (7th ed.) Citation

Alshami, Y., Hroub, O., Hroub, M., Abouodeh, S., Makhamre, Z., Hammouri, A. G., . . . Atawneh, O. (2025). Mitochondrial HMG‐CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant. Clinical Case Reports, 13(12), 1. https://doi.org/10.1002/ccr3.71622

Chicago Style (17th ed.) Citation

Alshami, Yasmeen, Osama Hroub, Mohammad Hroub, Saja Abouodeh, Zahra Makhamre, Ahmad G. Hammouri, Ibrahim Alzatari, and Osama Atawneh. "Mitochondrial HMG‐CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant." Clinical Case Reports 13, no. 12 (2025): 1. https://doi.org/10.1002/ccr3.71622.

MLA (9th ed.) Citation

Alshami, Yasmeen, et al. "Mitochondrial HMG‐CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant." Clinical Case Reports, vol. 13, no. 12, 2025, p. 1, https://doi.org/10.1002/ccr3.71622.