Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease

由 Schiff, E. R., Frampton, M., Ben-Yosef, N., Avila, B. E., Semplici, F., Pontikos, N., Bloom, S. L., McCartney, S. A., Vega, R., Lovat, L. B., Wood, E., Hart, A., Israeli, E., Crespi, D., Furman, M. A., Mann, S., Murray, C. D., Segal, A. W., Levine, A. P.
發表在 Hum Genet (2018)