Cite

    Chapleau, C. A., Lane, J., Kirwin, S., Schanen, C., Vinette, K. M. B., Stubbolo, D., MacLeod, P., Glaze, D. G., Motil, K. J., Neul, J. L., Skinner, S. A., Kaufmann, W. E., & Percy, A. K. (n.d.). erratum to "Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome", Am J Med Genet Part A 161A:1638–1646. American journal of medical genetics, 164(5), 1346. http://access.bl.uk/ark:/81055/vdc_100024958103.0x00002d