Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome (Scientific Reports, (2017), 7, 1, (12288), 10.1038/s41598-017-11620-3)

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Abstract

This Article contains an error in the Acknowledgements section. “We thank all patients and their families who contribute to this study. The work was supported by grants from the Spanish Ministry of Health (Instituto de Salud Carlos III/FEDER, PI15/01013); Crowdfunding program PRECIPITA, from the Spanish Ministry of Health (Fundación Española para la Ciencia y la Tecnología); Catalan Association for Rett Syndrome; Fondobiorett and Mi Princesa Rett.”should read: “We thank all patients and their families who contribute to this study. The work was supported by grants from the Spanish Ministry of Health (Instituto de Salud Carlos III/FEDER, PI15/01159); Crowdfunding program PRECIPITA, from the Spanish Ministry of Health (Fundación Española.

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CITATION STYLE

APA

Vidal, S., Brandi, N., Pacheco, P., Gerotina, E., Blasco, L., Trotta, J. R., … Villar, C. (2021, December 1). Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome (Scientific Reports, (2017), 7, 1, (12288), 10.1038/s41598-017-11620-3). Scientific Reports. Nature Research. https://doi.org/10.1038/s41598-021-97262-y

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