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Q28943547-48D0DA99-B2FC-40EA-9FE1-4E6531325E1E
Q28943547-48D0DA99-B2FC-40EA-9FE1-4E6531325E1E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28943547-48D0DA99-B2FC-40EA-9FE1-4E6531325E1E
Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation
P921
Q28943547-48D0DA99-B2FC-40EA-9FE1-4E6531325E1E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28943547-48D0DA99-B2FC-40EA-9FE1-4E6531325E1E
rank
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type
BestRank
Statement
P921
genome-wide association study