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The effect of the nonpeptide neurotrophic compound SR 57746A on the progression of the disease state of the pmn mouse
1. The progressive motor neuronopathy (pmn) mouse is an autosomal recessive mutant, in which the homozygotes suffer caudio-cranial degeneration of motor axons and die several weeks after birth. This strain provides the opportunity of testing potential therapeutic strategies for the treatment of moto...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
1998
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1565442/ https://ncbi.nlm.nih.gov/pubmed/9690875 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjp.0701885 |
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