Correction: Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G
Mónica Mora-Gómez, Marta Feito, Natalia Gallego-Zazo, Rocío Maseda-Pedrero, Tristán G. Sobral-Costas, Lucía Miranda-Alcaraz, Valeria Vásquez-Amell, Manuel Rodríguez-Canó, Alejandro Parra, Mario Cazalla, Pedro Arias, Cristina Silván, Juan A. Jiménez-Estrada, Víctor L. Ruiz-Pérez
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsSkin and Cellular Biology Research · Wnt/β-catenin signaling in development and cancer · Sympathectomy and Hyperhidrosis Treatments
An incorrect Funding statement was provided. The funding information was incomplete. The correct funding statement reads:
“The author(s) declared that financial support was received for this work and/or its publication. This study has been funded by Instituto de Salud Carlos III through the projects PMP21/00063 and PMP22/00049 and by Next Generation EU funds, which finance the actions of the Recovery and Resilience Facility (RRF).”
The original version of this article has been updated.