Published 1996 | Version v1.0.0
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Hallervorden-Spatz Disease: Clinicopathology

Abstract

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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PNB-10-31-a

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Created
1996
When the item was originally created.