In this issue, Lai-Cheong et al. report a patient with Kindler syndrome who showed revertant mosaicism: a patch of normal-looking skin attributable to a reverse mutation. The molecular basis of the reverted patch appeared to be the deletion of a duplicated cytosine, thus restoring the reading frame of FERMT1 transcripts. This finding further pushes the frontier of revertant mosaicism, a phenomenon of spontaneous gene repair, which can be seen with the naked eye in skin. © 2012 The Society for Investigative Dermatology.
CITATION STYLE
Jonkman, M. F., & Pasmooij, A. M. G. (2012). Realm of revertant mosaicism expanding. Journal of Investigative Dermatology. Nature Publishing Group. https://doi.org/10.1038/jid.2011.445
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