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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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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

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