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Q37325277-17C471BE-F655-481E-B19E-4C893EDBBEA4
Q37325277-17C471BE-F655-481E-B19E-4C893EDBBEA4
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http://www.wikidata.org/entity/statement/Q37325277-17C471BE-F655-481E-B19E-4C893EDBBEA4
Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8.
P2860
Q37325277-17C471BE-F655-481E-B19E-4C893EDBBEA4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37325277-17C471BE-F655-481E-B19E-4C893EDBBEA4
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wasDerivedFrom
b409de91b083952febfe604a1ac2a3ca999d832a
P2860
Decreased cellular uptake and metabolism in Allan-Herndon-Dudley syndrome (AHDS) due to a novel mutation in the MCT8 thyroid hormone transporter.