APA (7th ed.) Citation

Merdler-Rabinowicz, R., Jacob, N., Breilyn, M., Morava, E., & Ganesh, J. (2026). Rapid genome sequencing clarifies the cause of severe neonatal hyper-CKemia in an infant at genetic risk for VLCAD deficiency. Molecular Genetics & Metabolism, 148(1), N.PAG. https://doi.org/10.1016/j.ymgme.2026.110043

Chicago Style (17th ed.) Citation

Merdler-Rabinowicz, Rona, Neil Jacob, Margo Breilyn, Eva Morava, and Jaya Ganesh. "Rapid Genome Sequencing Clarifies the Cause of Severe Neonatal Hyper-CKemia in an Infant at Genetic Risk for VLCAD Deficiency." Molecular Genetics & Metabolism 148, no. 1 (2026): N.PAG. https://doi.org/10.1016/j.ymgme.2026.110043.

MLA (9th ed.) Citation

Merdler-Rabinowicz, Rona, et al. "Rapid Genome Sequencing Clarifies the Cause of Severe Neonatal Hyper-CKemia in an Infant at Genetic Risk for VLCAD Deficiency." Molecular Genetics & Metabolism, vol. 148, no. 1, 2026, p. N.PAG, https://doi.org/10.1016/j.ymgme.2026.110043.