Modeling spinal muscular atrophy in Drosophila.

Spinal Muscular Atrophy (SMA), a recessive hereditary neurodegenerative disease in humans, has been linked to mutations in the survival motor neuron (SMN) gene. SMA patients display early onset lethality coupled with motor neuron loss and skeletal muscle atrophy. We used Drosophila, which encodes a...

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Bibliographic Details
Main Authors: Chang, H, Dimlich, D, Yokokura, T, Mukherjee, A, Kankel, M, Sen, A, Sridhar, V, Fulga, T, Hart, A, Van Vactor, D, Artavanis-Tsakonas, S
Format: Journal article
Language:English
Published: Public Library of Science 2008