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Survival motor Neuron protein regulates apoptosis in anin vitromodel of Spinal muscular atrophy

✍ Scribed by Graham C. Parker; Xingli Li; Roumen A. Anguelov; Gabor Toth; Adam Cristescu; Gyula Acsadi

Publisher
Springer-Verlag
Year
2008
Tongue
English
Weight
407 KB
Volume
13
Category
Article
ISSN
1029-8428

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## Abstract The hereditary neurodegenerative disease spinal muscular atrophy (SMA) with childhood onset is one of the most common genetic causes of infant mortality. The disease is characterized by selective loss of spinal cord motor neurons leading to muscle atrophy and is the result of mutations