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Novel monoamine oxidase A knock out mice with human-like spontaneous mutation
A novel line of mutant mice [monoamine oxidase A knockout (MAOA(A863T) KO)] harboring a spontaneous point nonsense mutation in exon 8 of the MAO A gene was serendipitously identified in a 129/SvEvTac colony. This mutation is analogous to the cause of a rare human disorder, Brunner syndrome, characte...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3435113/ https://ncbi.nlm.nih.gov/pubmed/18418249 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WNR.0b013e3282fd6e88 |
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