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Q24300196-4A2C093D-2BE7-4487-B371-90F98567A821
Q24300196-4A2C093D-2BE7-4487-B371-90F98567A821
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Statement
http://www.wikidata.org/entity/statement/Q24300196-4A2C093D-2BE7-4487-B371-90F98567A821
A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia
P2860
Q24300196-4A2C093D-2BE7-4487-B371-90F98567A821
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24300196-4A2C093D-2BE7-4487-B371-90F98567A821
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wasDerivedFrom
7c0842f6d26fcd2a9fdc2c8c1eb4f5b177be52bf
P2860
Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria.