Published 1989
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Journal Article
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Neuroaxonal Dystrophy
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Abstract
The clinical, pathological and biochemical findings in two brothers with a newly recognized form of infantile neuroaxonal dystrophy associated with alpha-N-acetylgalactosaminidase deficiency are reported from the Divisions of Medical and Molecular Genetics and Neuropathology, Mount Sinai School of Medicine, New York; Department of Chemistry, University of Alberta, Edmonton, Canada; Department of Physiological Chemistry, University of Bonn, Federal Republic of Germany; and Department of Hunan Genetics, University of Wurzburg, Federal Republic of Germany.Files
PNB-3-43.pdf
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(2.6 MB)
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- PNB-3-43
Dates
- Created
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1989When the item was originally created.