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Radiofrequency ablation for DYT‐28 dystonia: short term follow‐up of three adult cases
Mutations in the lysine methyltransferase 2B (KMT2B) gene have recently been reported to be associated with childhood‐onset generalized dystonia. There have been no studies investigating ablative treatments for the management of this disorder. Three patients underwent either a staged unilateral pall...
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| Publicat a: | Ann Clin Transl Neurol |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7545596/ https://ncbi.nlm.nih.gov/pubmed/32886413 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51170 |
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