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Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms
Movement disorders comprise a group of heterogeneous diseases with often complex clinical phenotypes. Overlapping symptoms and a lack of diagnostic biomarkers may hamper making a definitive diagnosis. Next-generation sequencing techniques have substantially contributed to unraveling genetic etiologi...
Guardat en:
| Publicat a: | J Inherit Metab Dis |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Netherlands
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6326993/ https://ncbi.nlm.nih.gov/pubmed/29948482 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-018-0205-0 |
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