(Q41924213)
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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31
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4
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199-201
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Identifiers
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