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Over the past decade, molecular genetic investigations of neurologic disease have entered a veritable golden age. With the recent cloning of the genes for Huntington's disease, amyotrophic lateral sclerosis, and neurofibromatosis 1 and 2, among others, molecular-based studies of nervous-system disorders reached a new pinnacle. They not only serve as effective models for logically determining the etiologic basis of inherited maladies in humans, but also are beginning to confirm the momentous promise of molecular biology for eventually treating neurogenetic abnormalities. It is not surprising, then, that this field has progressed at a whirlwind pace. Even those who are deeply immersed
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