Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family
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Title
Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family
Authors
Keywords
Intellectual Disability, Intellectual Disability, Single Nucleotide Polymorphism Array, Whole Exome Sequencing, Pakistani Family
Journal
HUMAN GENETICS
Volume 133, Issue 8, Pages 975-984
Publisher
Springer Nature
Online
2014-03-12
DOI
10.1007/s00439-014-1438-0
References
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