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SMN is required for sensory-motor circuit function in Drosophila

Spinal muscular atrophy (SMA) is a lethal human disease characterized by motor neuron dysfunction and muscle deterioration due to depletion of the ubiquitous Survival Motor Neuron (SMN) protein. Drosophila SMN mutants have reduced muscle size and defective locomotion, motor rhythm and motor neuron n...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Imlach, Wendy L., Beck, Erin S., Choi, Ben Jiwon, Lotti, Francesco, Pellizzoni, Livio, McCabe, Brian D.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2012
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3475188/
https://ncbi.nlm.nih.gov/pubmed/23063130
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2012.09.011
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