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A Panel-Based Sequencing Analysis of Patients with Paget’s Disease of Bone Suggests Enrichment of Rare Genetic Variation in regulators of NF-κB Signaling and Supports the Importance of the 7q33 Locus

Crossref DOI link: https://doi.org/10.1007/s00223-021-00881-w

Published Online: 2021-06-25

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

De Ridder, Raphaël

Vandeweyer, Geert

Boudin, Eveline

Hendrickx, Gretl

Huybrechts, Yentl

Cremers, Tycho Canter

Devogelaer, Jean-Pierre

Mortier, Geert

Fransen, Erik

Van Hul, Wim https://orcid.org/0000-0002-5065-7858
Funding

Funding for this research was provided by:

Fonds Wetenschappelijk Onderzoek (1S07717N, 12A3814N)

Fonds Wetenschappelijk Onderzoek (12D1717N)

Research fund of the University of Antwerp (FFB190208)
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Text and Data Mining valid from 2021-06-25

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Article History

Received: 7 April 2021

Accepted: 15 June 2021

First Online: 25 June 2021

Declarations

:

: Raphaël De Ridder, Geert Vandeweyer, Eveline Boudin, Gretl Hendrickx, Yentl Huybrechts, Tycho Canter Cremers, Jean-Pierre Devogelaer, Geert Mortier, Erik Fransen and Wim Van Hul declares that they have no conflict of interest to disclose.

: All procedures involving human participants were performed in accordance with the ethical standards of the institutional and/or national research committee (Approval Number 300201731272) and with the Helsinki declaration and its later amendments or comparable ethical standards.

: For all patients an informed consent was obtained prior to the study.

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