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Q36169063-9BADFF2E-B09A-470E-AF08-4BADE7C0EED4
Q36169063-9BADFF2E-B09A-470E-AF08-4BADE7C0EED4
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http://www.wikidata.org/entity/statement/Q36169063-9BADFF2E-B09A-470E-AF08-4BADE7C0EED4
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.
P2860
Q36169063-9BADFF2E-B09A-470E-AF08-4BADE7C0EED4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36169063-9BADFF2E-B09A-470E-AF08-4BADE7C0EED4
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wasDerivedFrom
1399e61746a61deaefab008d5f350610eb8176e5
P2860
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss