Genetic alterations of δ-catenin/NPRAP/Neurojungin (CTNND2): functional implications in complex human diseases
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Title
Genetic alterations of δ-catenin/NPRAP/Neurojungin (CTNND2): functional implications in complex human diseases
Authors
Keywords
Autism Spectrum Disorder, Autism Spectrum Disorder, Copy Number Variation, Intellectual Disability, Myopia
Journal
HUMAN GENETICS
Volume 135, Issue 10, Pages 1107-1116
Publisher
Springer Nature
Online
2016-07-05
DOI
10.1007/s00439-016-1705-3
References
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