WHOLE EXOME SEQUENCING OF TWO RARE FAMILIAL COHORTS IDENTIFIES PUTATIVE GENETIC VARIANTS IN CHILDHOOD SJOGREN'S DISEASE

被引：0
|
作者：
Winn, N. [1 ]
Kim, S. [2 ]
Mun, S. [2 ]
Khan, Z. [1 ]
Thatayatikom, A. [3 ]
Han, K. [2 ]
Cha, S. [1 ]
机构：
[1] Univ Florida, Gainesville, FL USA
[2] Dankook Univ, Cheonan, South Korea
[3] AdventHlth Med Grp, Orlando, FL USA
来源：
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY | 2022年 / 40卷 / 12期
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D O I：
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
153
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页码：26 / 26
页数：1
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