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Q28588664-40D7C2AF-9B46-4542-A5C8-3CE9FC24CB48
Q28588664-40D7C2AF-9B46-4542-A5C8-3CE9FC24CB48
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-40D7C2AF-9B46-4542-A5C8-3CE9FC24CB48
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
P2860
Q28588664-40D7C2AF-9B46-4542-A5C8-3CE9FC24CB48
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-40D7C2AF-9B46-4542-A5C8-3CE9FC24CB48
rank
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wasDerivedFrom
04bac335be7845d5b5ed1fa7156111bf2280396f
P2860
Prader-Willi syndrome: current understanding of cause and diagnosis.