Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2
Open Access
- 1 January 2017
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 19 (1), 13-19
- https://doi.org/10.1038/gim.2016.42
Abstract
No abstract availableKeywords
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