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Q48624376-3E5AAC92-19CF-438F-B842-55AD0BA767B6
Q48624376-3E5AAC92-19CF-438F-B842-55AD0BA767B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48624376-3E5AAC92-19CF-438F-B842-55AD0BA767B6
Novel CLCNKB mutations causing Bartter syndrome affect channel surface expression.
P2860
Q48624376-3E5AAC92-19CF-438F-B842-55AD0BA767B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48624376-3E5AAC92-19CF-438F-B842-55AD0BA767B6
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wasDerivedFrom
ac6b227bd24e56f153dfce17baaf75cdf1222ba2
P2860
Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia.