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APA Citation
Wheeler, P. G., Ng, B. G., Sanford, L., Sutton, V. R., Bartholomew, D. W., Pastore, M. T., Bamshad, M. J., Kircher, M., Buckingham, K. J., Nickerson, D. A., Shendure, J., & Freeze, H. H. (2016). sRD5A3‐CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features. American journal of medical genetics, 170(12), 3165–3171. http://access.bl.uk/ark:/81055/vdc_100039241562.0x00003d