Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
- 1 January 2017
- journal article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 19 (1), 53-61
- https://doi.org/10.1038/gim.2016.54
Abstract
No abstract availableKeywords
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