Familial Angelman syndrome with atypical phenotype due to a new mutation in the UBE3A gene

被引：0
|
作者：
van der Burgt, I [1 ]
Nillesen, W [1 ]
van Buggenhout, G [1 ]
Sistermans, E [1 ]
机构：
[1] Acad Med Hosp, Dept Clin Genet, Maastricht, Netherlands
来源：
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH | 2004年 / 48卷
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中图分类号：
G76 [特殊教育];
学科分类号：
040109 ;
摘要：
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页码：287 / 287
页数：1
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