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Q37717896-8B316A9B-BF95-4F30-B4E9-86F18E5226CF
Q37717896-8B316A9B-BF95-4F30-B4E9-86F18E5226CF
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http://www.wikidata.org/entity/statement/Q37717896-8B316A9B-BF95-4F30-B4E9-86F18E5226CF
Chronic Enzyme Replacement to the Brain of a Late Infantile Neuronal Ceroid Lipofuscinosis Mouse Has Differential Effects on Phenotypes of Disease.
P2860
Q37717896-8B316A9B-BF95-4F30-B4E9-86F18E5226CF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37717896-8B316A9B-BF95-4F30-B4E9-86F18E5226CF
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type
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wasDerivedFrom
426215cb6a7dd498bef90e8f92e280bcb8c9d81e
P2860
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).