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Q48363172-27245CE5-6673-4922-B128-97F87342B3CE
Q48363172-27245CE5-6673-4922-B128-97F87342B3CE
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http://www.wikidata.org/entity/statement/Q48363172-27245CE5-6673-4922-B128-97F87342B3CE
Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome.
P2860
Q48363172-27245CE5-6673-4922-B128-97F87342B3CE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48363172-27245CE5-6673-4922-B128-97F87342B3CE
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wasDerivedFrom
d21505ddd8bc99faf0fe7e28a8105577cce150ff
P2860
Novel CLCNKB mutations causing Bartter syndrome affect channel surface expression.