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Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes

The Original Article was published on 03 February 2016

Correction to: Molecular Cytogenetics (2016) 9:10 https://doi.org/10.1186/s13039-016-0219-y

Following publication of the original article [1], an error was identified in the article title: the gene name NFIA was incorrectly captured as NIFA. The article title has been updated above and in the original article.

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  1. 1.

    Coci EC, et al. CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes. Mol Cytogenet. 2016;9:10. https://doi.org/10.1186/s13039-016-0219-y.

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Correspondence to Emanuele G. Coci.

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Coci, E.G., Koehler, U., Liehr, T. et al. Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes. Mol Cytogenet 14, 17 (2021). https://doi.org/10.1186/s13039-021-00534-5

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