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Dive into the research topics of 'Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2'. Together they form a unique fingerprint.- Sort by
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Samin A. Sajan, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, James R. Lupski, Daniel G. Glaze, Walter E. Kaufmann, Steven A. Skinner, Fran Annese, Michael J. Friez, Jane Lane, Alan K. Percy, Jeffrey L. Neul
Research output: Contribution to journal › Article › peer-review