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Q34468937-36376C4F-608D-4D1A-B62D-19F5343AD135
Q34468937-36376C4F-608D-4D1A-B62D-19F5343AD135
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34468937-36376C4F-608D-4D1A-B62D-19F5343AD135
Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).
P2860
Q34468937-36376C4F-608D-4D1A-B62D-19F5343AD135
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34468937-36376C4F-608D-4D1A-B62D-19F5343AD135
rank
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Statement
wasDerivedFrom
6ea65fbef147e432cd628694d284d161db7b6d72
P2860
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome