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Q33382216-9CC9C2AB-7139-4329-A6D2-70721C2E856D
Q33382216-9CC9C2AB-7139-4329-A6D2-70721C2E856D
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Statement
http://www.wikidata.org/entity/statement/Q33382216-9CC9C2AB-7139-4329-A6D2-70721C2E856D
Transfection of the mutant MYH9 cDNA reproduces the most typical cellular phenotype of MYH9-related disease in different cell lines.
P2860
Q33382216-9CC9C2AB-7139-4329-A6D2-70721C2E856D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33382216-9CC9C2AB-7139-4329-A6D2-70721C2E856D
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wasDerivedFrom
571072c04d9f72e88c82e658d26fea9921eca3df
P2860
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness.