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Q36451472-2DBF58CF-E488-4E11-9DD9-66A0F2193972
Q36451472-2DBF58CF-E488-4E11-9DD9-66A0F2193972
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36451472-2DBF58CF-E488-4E11-9DD9-66A0F2193972
Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia.
P2860
Q36451472-2DBF58CF-E488-4E11-9DD9-66A0F2193972
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36451472-2DBF58CF-E488-4E11-9DD9-66A0F2193972
rank
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type
BestRank
Statement
wasDerivedFrom
9c884290914b6d08816bd8174604e8964ab9671a
P2860
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18)