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A functional variant of the dopamine D(3) receptor is associated with risk and age-at-onset of essential tremor
Familial essential tremor (ET), the most common inherited movement disorder, is generally transmitted as an autosomal dominant trait. A genome-wide scan for ET revealed one major locus on chromosome 3q13. Here, we report that the Ser9Gly variant in the dopamine D(3) receptor gene (DRD3), localized o...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1502303/ https://ncbi.nlm.nih.gov/pubmed/16809426 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0508189103 |
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