Autosomal dominant complex hereditary spastic paraplegia due to mutations in Spastin gene (Q100925): Difference between revisions
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CID11:ID_92075119 | |||
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Revision as of 17:42, 16 August 2026
No description defined
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_92075119 |
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| English | Autosomal dominant complex hereditary spastic paraplegia due to mutations in Spastin gene |
No description defined |
Statements
CID11:ID_92075119
0 references
