Hallervorden-Spatz Disease: Clinicopathology
Clinical and pathological features of familial late infantile Hallervorden-Spatz disease (HSD) are reported in two sisters, one of whom died at 11 years, from the Institute for Neurological Sciences, University of Siena, Italy.
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Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
1996-04-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
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Copy 1 | Available |