Harp Syndrome
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.
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Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
1995-04-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
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Copy 1 | Available |