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Erratum to “Detection of rarely identified multiple mutations inMECP2gene do not contribute to enhanced severity in Rett syndrome”, Am J Med Genet Part A 161A:1638-1646

Document Type

article

Author

Chapleau, Christopher A; Lane, Jane; Kirwin, Susan; Schanen, Carolyn; Vinette, Kathy MB; Stubbolo, Danielle; MacLeod, Patrick; Glaze, Daniel G; Motil, Kathleen J; Neul, Jeffrey L; Skinner, Steven A; Kaufmann, Walter E; Percy, Alan K

Source

American Journal of Medical Genetics Part A. 164(5)

Subject

Clinical Sciences
Genetics

Language

Online Access

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