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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326993/ https://www.ncbi.nlm.nih.gov/pubmed/29948482 http://dx.doi.org/10.1007/s10545-018-0205-0 |