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Q46145781-BB1664DD-D9B8-4CE2-B07E-DDB5E9F0289B
Q46145781-BB1664DD-D9B8-4CE2-B07E-DDB5E9F0289B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46145781-BB1664DD-D9B8-4CE2-B07E-DDB5E9F0289B
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).
P2860
Q46145781-BB1664DD-D9B8-4CE2-B07E-DDB5E9F0289B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46145781-BB1664DD-D9B8-4CE2-B07E-DDB5E9F0289B
rank
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wasDerivedFrom
ff2e33fbe6eb4d837ed858d1d75731ca43ff6c99
P2860
Autosomal recessive cerebellar ataxias: the current state of affairs.