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APA Citation

    Chen, L. A., Kim, M., Li, D., Aita, R., Cataldo, S., Radin, A., Baylor, J., Deng, L., Hahn, B., Wong, K., Tin, K., Mengesha, E., & McGovern, D. (n.d.). wHOLE EXOME SEQUENCING OF A MULTIPLEX CROHN'S DISEASE FAMILY IDENTIFIES RARE ALTERATIONS IN PYGB ANDXRN2 AS POTENTIALLY HIGH IMPACT RISK VARIANTS OF DISEASE. Inflammatory bowel diseases, 29, S40. http://access.bl.uk/ark:/81055/vdc_100176521033.0x00000b
  
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