Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family
出版年份 2014 全文链接
标题
Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family
作者
关键词
Intellectual Disability, Intellectual Disability, Single Nucleotide Polymorphism Array, Whole Exome Sequencing, Pakistani Family
出版物
HUMAN GENETICS
Volume 133, Issue 8, Pages 975-984
出版商
Springer Nature
发表日期
2014-03-12
DOI
10.1007/s00439-014-1438-0
参考文献
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