Autosomal dominant pure hereditary spastic paraplegia due to mutations in Spastin gene (Q100868)
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No description defined
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1328224522 |
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| English | Autosomal dominant pure hereditary spastic paraplegia due to mutations in Spastin gene |
No description defined |
