Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease). (Q46145781)
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scientific article published on 11 March 2013
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease). |
scientific article published on 11 March 2013 |
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Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease). (English)
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Ben Oostra
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Rowida Almomani
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Guido J Breedveld
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Gijs W E Santen
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Emmelien Aten
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Dirk J Lefeber
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Jorrit I Hoff
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Esther Brusse
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Frans W Verheijen
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Marjolein Kriek
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Martijn H Breuning
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Monique Losekoot
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Johan T den Dunnen
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Bart P van de Warrenburg
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Anneke J A Maat-Kievit
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11 March 2013
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34
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706-713
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5
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