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Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease
We have examined several aspects of neurotransmitter function in the brains of mice carrying a deletion mutation in the gene encoding the purine salvage enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT). During the first 6 weeks of postnatal development, dopamine levels in whole-brain ext...
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| Опубликовано в: : | J Neurosci |
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| Главные авторы: | , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Society for Neuroscience
1994
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6577527/ https://ncbi.nlm.nih.gov/pubmed/7509865 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.14-03-01164.1994 |
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