Parkin disease: a clinicopathologic entity?
<br xmlns:etd="http://www.ouls.ox.ac.uk/ora/modsextensions"><strong>Importance: </strong>Mutations in the gene encoding parkin (PARK2) are the most common cause of autosomal recessive juvenile-onset and young-onset parkinsonism. The few available detailed neuropathologic...
| Main Authors: | , , , , , , , , , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
American Medical Association
2013
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