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Q34682504-6EFC4A60-DF7E-4B95-A191-49B502856498
Q34682504-6EFC4A60-DF7E-4B95-A191-49B502856498
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http://www.wikidata.org/entity/statement/Q34682504-6EFC4A60-DF7E-4B95-A191-49B502856498
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.
P2860
Q34682504-6EFC4A60-DF7E-4B95-A191-49B502856498
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34682504-6EFC4A60-DF7E-4B95-A191-49B502856498
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wasDerivedFrom
75a9a057b157aefeb72b9fc43538681de36b6b28
P2860
Liddle's syndrome mutations increase Na+ transport through dual effects on epithelial Na+ channel surface expression and proteolytic cleavage.