SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause.
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| Title: | SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause. |
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| Authors: | Arlt, Annabelle1,2 (AUTHOR), Akova-Öztürk, Esra2 (AUTHOR), Schirmacher, Anja3 (AUTHOR), Schlüter, Bernhard3 (AUTHOR), Rust, Stephan3,4 (AUTHOR), Meyer zu Hörste, Gerd2 (AUTHOR), Wiendl, Heinz2 (AUTHOR), Wiethoff, Sarah2,5 (AUTHOR) sarah.wiethoff@ukmuenster.de |
| Source: | Journal of Neurogenetics. Jun2024, Vol. 38 Issue 2, p35-40. 6p. |
| Database: | Academic Search Ultimate |
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| ISSN: | 01677063 |
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| DOI: | 10.1080/01677063.2024.2374898 |
