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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Bibliografski detalji
Glavni autori: 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
Jezik:English
Izdano: Public Library of Science 2008