Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance

Authors: Fatemeh Ghorbani, Mohamed Z. Alimohamed, Juliana F. Vilacha, Krista K. Van Dijk, Jelkje De Boer-Bergsma, Michiel R. Fokkens, Henny Lemmink, Rolf H. Sijmons, Birgit Sikkema-Raddatz, Matthew R. Groves, Corien C. Verschuuren-Bemelmans, Dineke S. Verbeek, Cleo C. Van Diemen, Helga Westers

Source: Frontiers in Genetics, Vol 13 (2022)

Subject Terms: genetic diagnostics, variant of unknown significance, spinocerebellar ataxia, gene panel, functional studies, protein modeling, Genetics, QH426-470

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2022.782685/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/e0ce2a4a56bf4a8db0790dfc9826b968