Disorders of the motor neuron are etiologically and clinically heterogeneous and cause serious disability and death. Whereas mendelian inheritance can be demonstrated in a subset of these disorders, the genetic contribution to the sporadic forms of motor neuron degeneration are not well understood. In families with spinal muscular atrophy, Kennedy disease and amyotrophic lateral sclerosis, genetic linkage analysis and positional cloning have proven to be extremely productive. The genetics of these neurodegenerative disorders are reviewed.
机构:Division of Neuropathology, Department of Pathology, University of North Carolina at Chapel Hill, Chapel Hill, 27599-7525, NC, CB No. 7525, Brinkhous-Bullitt Building
MURAYAMA, S
BOULDIN, TW
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机构:Division of Neuropathology, Department of Pathology, University of North Carolina at Chapel Hill, Chapel Hill, 27599-7525, NC, CB No. 7525, Brinkhous-Bullitt Building
BOULDIN, TW
SUZUKI, K
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机构:Division of Neuropathology, Department of Pathology, University of North Carolina at Chapel Hill, Chapel Hill, 27599-7525, NC, CB No. 7525, Brinkhous-Bullitt Building
机构:Division of Neuropathology, Department of Pathology, University of North Carolina at Chapel Hill, Chapel Hill, 27599-7525, NC, CB No. 7525, Brinkhous-Bullitt Building
MURAYAMA, S
BOULDIN, TW
论文数: 0引用数: 0
h-index: 0
机构:Division of Neuropathology, Department of Pathology, University of North Carolina at Chapel Hill, Chapel Hill, 27599-7525, NC, CB No. 7525, Brinkhous-Bullitt Building
BOULDIN, TW
SUZUKI, K
论文数: 0引用数: 0
h-index: 0
机构:Division of Neuropathology, Department of Pathology, University of North Carolina at Chapel Hill, Chapel Hill, 27599-7525, NC, CB No. 7525, Brinkhous-Bullitt Building