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).
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| Description | scientific article published on 11 March 2013 |
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author: Frans W Verheijen Ben A Oostra Esther Brusse Yu Sun Robert M Verdijk |
| Publication date | March 11, 2013 |
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