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Q26738455-2D1CB403-E00D-4A74-8F86-C546B62454AE
Q26738455-2D1CB403-E00D-4A74-8F86-C546B62454AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26738455-2D1CB403-E00D-4A74-8F86-C546B62454AE
Ultra-rare Disease and Genomics-Driven Precision Medicine
P2860
Q26738455-2D1CB403-E00D-4A74-8F86-C546B62454AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26738455-2D1CB403-E00D-4A74-8F86-C546B62454AE
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wasDerivedFrom
26f01b8f867223eed9349f7c942e52487a9f30da
P2860
Rare cases of congenital arthrogryposis multiplex caused by novel recurrent CHRNG mutations.