EXPANDING THE PHENOTYPE OF RARE X-LIKNKED INTELLECTUAL DISABILITY SYNDROME CAUSED BY UPF3B GENE

被引：0
|
作者：
Haanpaa, M. K.
Koillinen, H.
Ignatius, J.
机构：
[1] Turku Univ Hosp, Turku, Finland
[2] Stanford Sch Med, Stanford, CA 94305 USA
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2020年 / 182卷 / 04期
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D O I：
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中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
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页码：911 / 912
页数：2
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