Published 1995
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Harp Syndrome
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Abstract
Harp syndrome, characterized by hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration, is described in three patients from the National Hospital, Queen Square, London, Newcastle General Hospital, and the Royal Free Hospital, London, UK.Files
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- PNB-9-26-b
Dates
- Created
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1995When the item was originally created.