A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL. (Q41924213)
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scientific article published on August 2000
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL. |
scientific article published on August 2000 |
Statements
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A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL. (English)
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Simonati A
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Santorum E
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Tessa A
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Polo A
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Simonetti F
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Bernardina BD
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Santorelli FM
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Rizzuto N
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1 August 2000
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Identifiers
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