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Excessive mobility interrupted

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  • Lorenz Studer

    (Lorenz Studer is in the Center for Stem Cell Biology, Developmental Biology Program, Sloan-Kettering Institute for Cancer Research, New York, New York 10065, USA. studerl@mskcc.org)

Abstract

Mobile DNA sequences called L1 contribute to the brain's genetic heterogeneity and may affect neuron function. The protein MeCP2, which is mutated in Rett syndrome, seems to regulate the activity of these genomic elements. See Letter p.443

Suggested Citation

  • Lorenz Studer, 2010. "Excessive mobility interrupted," Nature, Nature, vol. 468(7322), pages 383-384, November.
    • Handle: RePEc:nat:nature:v:468:y:2010:i:7322:d:10.1038_468383a
    DOI: 10.1038/468383a
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