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Q40600626-9B6BBB91-1C8F-4360-B5EC-3B566D2C062C
Q40600626-9B6BBB91-1C8F-4360-B5EC-3B566D2C062C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40600626-9B6BBB91-1C8F-4360-B5EC-3B566D2C062C
Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux.
P2860
Q40600626-9B6BBB91-1C8F-4360-B5EC-3B566D2C062C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40600626-9B6BBB91-1C8F-4360-B5EC-3B566D2C062C
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Statement
wasDerivedFrom
1901dc3af762c0196ba6706a3181f59921c0aa2b
P2860
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)