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Role of upper motor neuron functions in neuromuscular weaknesses in spinal muscular atrophies

✍ Scribed by I. Hausmanowa-Petrusewicz; M.R. Dimitrijević


Book ID
115868574
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
121 KB
Volume
75
Category
Article
ISSN
0013-4694

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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