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Q36169063-8A8FB430-0865-4610-BF7A-197E75672C1B
Q36169063-8A8FB430-0865-4610-BF7A-197E75672C1B
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http://www.wikidata.org/entity/statement/Q36169063-8A8FB430-0865-4610-BF7A-197E75672C1B
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.
P2860
Q36169063-8A8FB430-0865-4610-BF7A-197E75672C1B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36169063-8A8FB430-0865-4610-BF7A-197E75672C1B
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wasDerivedFrom
9c461ff9a634dab308e94e1c34ef08f6e4ff5b96
P2860
Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes