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APA Citation
Werner, K. M., Cox, A. J., Qian, E., Jain, P., Ji, W., Tikhonova, I., Castaldi, C., Bilguvar, K., Knight, J., Ferdinandusse, S., Fawaz, R., Jiang, Y., Gallagher, P. G., Bizzarro, M., Gruen, J. R., Bale, A., & Zhang, H. (2022). d‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. American journal of medical genetics, 188(1), 357–363. http://access.bl.uk/ark:/81055/vdc_100147224897.0x00001e