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Q34824796-408AA62E-C74D-40D0-99B2-0C2486BEBCB8
Q34824796-408AA62E-C74D-40D0-99B2-0C2486BEBCB8
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Statement
http://www.wikidata.org/entity/statement/Q34824796-408AA62E-C74D-40D0-99B2-0C2486BEBCB8
Mice homozygous for c.451C>T mutation in Cln1 gene recapitulate INCL phenotype.
P2860
Q34824796-408AA62E-C74D-40D0-99B2-0C2486BEBCB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34824796-408AA62E-C74D-40D0-99B2-0C2486BEBCB8
rank
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type
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Statement
wasDerivedFrom
997ed7bc460fda78f156af0a6553cce9e33f3cdc
P2860
Infantile neuronal ceroid-lipofuscinosis (INCL): diagnostic criteria.