APA (7th ed.) Citation

KM, W., AJ, C., E, Q., P, J., W, J., I, T., . . . H, Z. (2022). D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. American journal of medical genetics. Part A, 188(1), 357. https://doi.org/10.1002/ajmg.a.62520

Chicago Style (17th ed.) Citation

KM, Werner, et al. "D-bifunctional Protein Deficiency Caused by Splicing Variants in a Neonate with Severe Peroxisomal Dysfunction and Persistent Hypoglycemia." American Journal of Medical Genetics. Part A 188, no. 1 (2022): 357. https://doi.org/10.1002/ajmg.a.62520.

MLA (9th ed.) Citation

KM, Werner, et al. "D-bifunctional Protein Deficiency Caused by Splicing Variants in a Neonate with Severe Peroxisomal Dysfunction and Persistent Hypoglycemia." American Journal of Medical Genetics. Part A, vol. 188, no. 1, 2022, p. 357, https://doi.org/10.1002/ajmg.a.62520.