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APA Citation
Reid, E. S., Williams, H., Anderson, G., Benatti, M., Chong, K., James, C., Ocaka, L., , , Hemingway, C., Little, D., Brown, R., Parker, A., Holden, S., Footitt, E., Rahman, S., Gissen, P., Mills, P. B., & Clayton, P. T. (2017). mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay. Journal of inherited metabolic disease, 40(3), 385–394. http://access.bl.uk/ark:/81055/vdc_100079074560.0x000044