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Q28588664-43B29635-D4EC-446C-BE62-D0F2B6950FBF
Q28588664-43B29635-D4EC-446C-BE62-D0F2B6950FBF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-43B29635-D4EC-446C-BE62-D0F2B6950FBF
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
P2860
Q28588664-43B29635-D4EC-446C-BE62-D0F2B6950FBF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-43B29635-D4EC-446C-BE62-D0F2B6950FBF
rank
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type
BestRank
Statement
wasDerivedFrom
04bac335be7845d5b5ed1fa7156111bf2280396f
P2860
Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy