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

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作者：
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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来源：
GASTROENTEROLOGY | 2023年 / 164卷 / 06期
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暂无
中图分类号：
R57 [消化系及腹部疾病];
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摘要：
Sa1800
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页码：S437 / S437
页数：1
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