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Q28588664-42EC1DCB-E908-4C06-A4F9-F66B4470A252
Q28588664-42EC1DCB-E908-4C06-A4F9-F66B4470A252
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-42EC1DCB-E908-4C06-A4F9-F66B4470A252
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
P2860
Q28588664-42EC1DCB-E908-4C06-A4F9-F66B4470A252
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-42EC1DCB-E908-4C06-A4F9-F66B4470A252
rank
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type
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wasDerivedFrom
04bac335be7845d5b5ed1fa7156111bf2280396f
P2860
The hereditary spastic paraplegias: nine genes and counting.