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Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity
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| Publicat a: | Mov Disord Clin Pract |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley & Sons, Inc.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7328426/ https://ncbi.nlm.nih.gov/pubmed/32626811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12961 |
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