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. 2014 Oct 13;23(24):6695. doi: 10.1093/hmg/ddu496

Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome

Dag H Yasui, Michael L Gonzales, Justin O Aflatooni, Florence K Crary, Daniel J Hu, Bryant J Gavino, Mari S Golub, John B Vincent, N Carolyn Schanen, Carl O Olson, Mojgan Rastegar, Janine M Lasalle
PMCID: PMC4311188

Human Molecular Genetics 2014 23:9; pp. 2447–2458; doi: 10.1093/hmg/ddt640

The ninth co-author's name was wrongly tagged in this paper. It is shown correctly above and has also been corrected online.

The authors apologise for this error.

Articles from Human Molecular Genetics are provided here courtesy of Oxford University Press

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