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Genome-Wide Expression Analysis of a Spinal Muscular Atrophy Model: Towards Discovery of New Drug Targets
Spinal Muscular Atrophy is a recessive genetic disease and affects lower motor neurones and muscle tissue. A single gene is disrupted in SMA: SMN1 activity is abolished but a second copy of the gene (SMN2) provides limited activity. While the SMN protein has been shown to function in the assembly of...
Autores principales: | Lee, Sheena, Sayin, Arzu, Grice, Stuart, Burdett, Howard, Baban, Dilair, van den Heuvel, Marcel |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151137/ https://www.ncbi.nlm.nih.gov/pubmed/18167563 http://dx.doi.org/10.1371/journal.pone.0001404 |
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