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Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome
BACKGROUND: Genes involved in Tourette syndrome (TS) remain largely unknown. We aimed to identify genetic factors contributing to TS in a French cohort of 120 individuals using a combination of hypothesis-driven and exome-sequencing approaches. METHODS: We first sequenced exons of SLITRK1-6 and HDC...
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| Publicado en: | Tremor Other Hyperkinet Mov (N Y) |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Columbia University Libraries/Information Services
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6878848/ https://ncbi.nlm.nih.gov/pubmed/31824749 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7916/tohm.v0.693 |
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