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Effect of genetic background on the phenotype of the Smn(2B/-) mouse model of spinal muscular atrophy
Spinal muscular atrophy (SMA) is caused by mutations or deletions in the Survival Motor Neuron 1 (SMN1) gene in humans. Modifiers of the SMA symptoms have been identified and genetic background has a substantial effect in the phenotype and survival of the severe mouse model of SMA. Previously, we ge...
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| Publicat a: | Hum Mol Genet |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5409218/ https://ncbi.nlm.nih.gov/pubmed/28172892 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw278 |
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