Sa1800 WHOLE EXOME SEQUENCING OF A MULTIPLEX CROHN'S DISEASE FAMILY IDENTIFIES RARE ALTERATIONS IN PYGB AND XRN2 AS POTENTIALLY HIGH IMPACT RISK VARIANTS OF DISEASE
| Autor: | Chen, Lea Ann, Kim, Minsuk, Li, Dalin, Aita, Rohit, Cataldo, Susan, Radin, Arielle, Baylor, Jessica, Deng, Lily, Hahn, Brett, Wong, Kevin, Tin, Kevin, Mengesha, Emebet, Mcgovern, Dermot P.B. |
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| Zdroj: | In Gastroenterology May 2023 164(6) Supplement:S |
| Databáze: | ScienceDirect |
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