Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan.

Spinal muscular atrophy is the most common genetic cause of infant mortality and is characterized by degeneration of lower motor neurons leading to muscle wasting. The causative gene has been identified as survival motor neuron (SMN). The invertebrate model organism Caenorhabditis elegans contains s...

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Bibliographic Details
Main Authors: Briese, M, Esmaeili, B, Fraboulet, S, Burt, E, Christodoulou, S, Towers, P, Davies, K, Sattelle, D
Format: Journal article
Language:English
Published: Oxford University Press 2009