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Abstract: A 4 page discussion of the epidemiology and testing mechanisms which are available for this autosomal recessive genetic mutation. The disease is characterized by severe degeneration of the Central Nervous System, a degeneration which most often manifests prior to the age of three but which can also be characterized by later onset. Testing to identify carriers of this disease is critical. Bibliography lists 4 sources.
Catagory: Disease, Treatment, & Epidemiology
Subcatagory: Medicine, Medical Issues, & Pharmacy
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