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Paroxysmal Dyskinesia in Children: from Genes to the Clinic
BACKGROUND AND PURPOSE: Paroxysmal dyskinesia is a genetically and clinically heterogeneous movement disorder. Recent studies have shown that it exhibits both phenotype and genotype overlap with other paroxysmal disorders as well as clinical heterogeneity. We investigated the clinical and genetic ch...
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| I publikationen: | J Clin Neurol |
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| Huvudupphovsmän: | , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Korean Neurological Association
2018
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6172489/ https://ncbi.nlm.nih.gov/pubmed/30198221 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3988/jcn.2018.14.4.492 |
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