| Title: |
SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause |
| Authors: |
Arlt, Annabelle; Akova-Öztürk, Esra; Schirmacher, Anja; Schlüter, Bernhard; Rust, Stephan; Meyer zu Hörste, Gerd; Wiendl, Heinz; Wiethoff, Sarah |
| Contributors: |
Ministry of Science, Research; Arts of Baden-Württemberg; European Social Fund (ESF) of Baden-Württemberg; UPS-NDDiag project from European Joint Programme Rare Disease |
| Source: |
Journal of Neurogenetics ; volume 38, issue 2, page 35-40 ; ISSN 0167-7063 1563-5260 |
| Publisher Information: |
Informa UK Limited |
| Publication Year: |
2024 |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| DOI: |
10.1080/01677063.2024.2374898 |
| Availability: |
https://doi.org/10.1080/01677063.2024.2374898; https://www.tandfonline.com/doi/pdf/10.1080/01677063.2024.2374898 |
| Rights: |
http://creativecommons.org/licenses/by/4.0/ |
| Accession Number: |
edsbas.BBC4029E |
| Database: |
BASE |