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APA Citation
Amor, D. J., Marsh, A. P., Storey, E., Tankard, R., Gillies, G., Delatycki, M. B., Pope, K., Bromhead, C., Leventer, R. J., Bahlo, M., & Lockhart, P. J. (2016). heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency. Neurology, 2, . http://access.bl.uk/ark:/81055/vdc_100040135769.0x000001