Mapping a shared genetic basis for neurodevelopmental disorders
Abstract Distinct neurodevelopmental disorders have a common genetic etiology that explains the high degree of comorbidity among these disorders. A recent study sought to identify copy number variants across five neurodevelopmental disorders, and detected an enrichment for chromosome 9p24.3 duplicat...
Main Authors: | Matthew Jensen, Santhosh Girirajan |
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Format: | Article |
Language: | English |
Published: |
BMC
2017-12-01
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Series: | Genome Medicine |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13073-017-0503-4 |
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