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Q48490299-1DE88BBF-8CFE-43F5-B91F-E83C7E0B0FC5
Q48490299-1DE88BBF-8CFE-43F5-B91F-E83C7E0B0FC5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48490299-1DE88BBF-8CFE-43F5-B91F-E83C7E0B0FC5
Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome.
P2860
Q48490299-1DE88BBF-8CFE-43F5-B91F-E83C7E0B0FC5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48490299-1DE88BBF-8CFE-43F5-B91F-E83C7E0B0FC5
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type
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Statement
wasDerivedFrom
900fa671f54b8ae44a6697c8fcf66692793d8703
P2860
X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8.