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Q46642721-C6F43741-C37B-465A-8D2B-970793659CD4
Q46642721-C6F43741-C37B-465A-8D2B-970793659CD4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46642721-C6F43741-C37B-465A-8D2B-970793659CD4
Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 gene.
P921
Q46642721-C6F43741-C37B-465A-8D2B-970793659CD4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46642721-C6F43741-C37B-465A-8D2B-970793659CD4
rank
NormalRank
type
BestRank
Statement
P921
Infantile neuronal ceroid lipofuscinosis