Article
Spinal muscular atrophy: mechanisms and therapeutic strategies.
Human molecular genetics - 15 Apr 2010
Lorson Christian L, Rindt Hansjorg, Shababi Monir
Abstract excerpt
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder and a leading genetic cause of infantile mortality. SMA is caused by mutation or deletion of Survival Motor Neuron-1 (SMN1). The clinical features of the disease are caused by specific degeneration of alpha-motor neurons in the spinal cord, leading to muscle weakness, atrophy and, in the majority of cases, premature death. A highly...
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