Erratum: An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015))

Haloom Rafehi, Justin Read, David J. Szmulewicz, Kayli C. Davies, Penny Snell, Liam G. Fearnley, Liam Scott, Mirja Thomsen, Greta Gillies, Kate Pope, Mark F. Bennett, Jacob E. Munro, Kathie J. Ngo, Luke Chen, Mathew J. Wallis, Ernest G. Butler, Kishore R. Kumar, Kathy HC Wu, Susan E. Tomlinson, Stephen TischAbhishek Malhotra, Matthew Lee-Archer, Egor Dolzhenko, Michael A. Eberle, Leslie J. Roberts, Brent L. Fogel, Norbert Brüggemann, Katja Lohmann, Martin B. Delatycki, Melanie Bahlo*, Paul J. Lockhart*

*Corresponding author for this work
5 Citations (Scopus)


(The American Journal of Human Genetics 110, 105–119; January 5, 2023) After publication of this article, the autosomal-dominant adult-onset ataxia the authors preliminarily called SCA50 was officially named SCA27B by OMIM. The title and text have now been updated to reflect this name change.

Original languageEnglish
JournalAmerican Journal of Human Genetics
Issue number6
Pages (from-to)1018
Number of pages1
Publication statusPublished - 01.06.2023

Research Areas and Centers

  • Research Area: Medical Genetics

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