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Q28263895-507FBC06-95CA-4857-9277-F88C1FEA782B
Q28263895-507FBC06-95CA-4857-9277-F88C1FEA782B
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Statement
http://www.wikidata.org/entity/statement/Q28263895-507FBC06-95CA-4857-9277-F88C1FEA782B
The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families
P2860
Q28263895-507FBC06-95CA-4857-9277-F88C1FEA782B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28263895-507FBC06-95CA-4857-9277-F88C1FEA782B
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wasDerivedFrom
24861d10ff21f89c0761902358657dbace82aa57
P2860
A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity