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Q40981091-ECE5A72A-8365-4942-BA5F-94462B38E5E9
Q40981091-ECE5A72A-8365-4942-BA5F-94462B38E5E9
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http://www.wikidata.org/entity/statement/Q40981091-ECE5A72A-8365-4942-BA5F-94462B38E5E9
Isolated congenital hepatic fibrosis associated with TMEM67 mutations: report of a new genotype-phenotype relationship.
P2860
Q40981091-ECE5A72A-8365-4942-BA5F-94462B38E5E9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40981091-ECE5A72A-8365-4942-BA5F-94462B38E5E9
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wasDerivedFrom
b425f5d75054865e1778f87ce108b08b5fc2a8d3
P2860
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.