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Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD

Lookup NU author(s): Professor Giorgio TascaORCiD

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).

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Author(s): Strafella C, Caputo V, Bortolani S, Torchia E, Megalizzi D, Trastulli G, Monforte M, Colantoni L, Caltagirone C, Ricci E, Tasca G, Cascella R, Giardina E

Publication type: Article

Publication status: Published

Journal: Frontiers in Genetics

Year: 2023

Volume: 14

Online publication date: 22/08/2023

Acceptance date: 09/08/2023

Date deposited: 07/09/2023

ISSN (electronic): 1664-8021

Publisher: Frontiers Media SA

URL: https://doi.org/10.3389/fgene.2023.1235589

DOI: 10.3389/fgene.2023.1235589

Data Access Statement: The datasets presented in this article are not readily available because data obtained from whole exome sequencing are sensitive and. our ethics committee does not authorize the sharing of these data. Requests to access the datasets should be directed to the corresponding author.

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