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

Saved in:
Bibliographic Details
Title: Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance.
Authors: Ghorbani F; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Alimohamed MZ; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.; Department of Hematology and Blood Transfusion, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.; Shree Hindu Mandal Hospital, Dar es Salaam, Tanzania., Vilacha JF; Groningen Biomolecular Sciences and Biotechnology Institute, Zernike Institute for Advanced Materials, University of Groningen, Groningen, Netherlands., Van Dijk KK; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., De Boer-Bergsma J; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Fokkens MR; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Lemmink H; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Sijmons RH; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Sikkema-Raddatz B; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Groves MR; Structural Biology in Drug Design, Department of Drug Design, Groningen Research Institute of Pharmacy, University of Groningen, Groningen, Netherlands., Verschuuren-Bemelmans CC; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Verbeek DS; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Van Diemen CC; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Westers H; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Source: Frontiers in genetics [Front Genet] 2022 Mar 25; Vol. 13, pp. 782685. Date of Electronic Publication: 2022 Mar 25 (Print Publication: 2022).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
Description
ISSN:1664-8021
DOI:10.3389/fgene.2022.782685