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Q38115191-89D0AEA3-2933-4DEA-8F1D-A7086472ABFC
Q38115191-89D0AEA3-2933-4DEA-8F1D-A7086472ABFC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38115191-89D0AEA3-2933-4DEA-8F1D-A7086472ABFC
Neuronal ceroid lipofuscinosis: impact of recent genetic advances and expansion of the clinicopathologic spectrum.
P2860
Q38115191-89D0AEA3-2933-4DEA-8F1D-A7086472ABFC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38115191-89D0AEA3-2933-4DEA-8F1D-A7086472ABFC
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NormalRank
type
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Statement
wasDerivedFrom
d7dc51288bb34b38ea0e023883f0fac98371b03f
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).