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APA Citation
Montalbano, A., Juergensen, L., Roeth, R., Weiss, B., Fukami, M., Fricke‐Otto, S., Binder, G., Ogata, T., Decker, E., Nuernberg, G., Hassel, D., & Rappold, G. A. (2016). retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. EMBO molecular medicine, 8(12), 1455–1469. http://access.bl.uk/ark:/81055/vdc_100039631576.0x00002e