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Q40981091-48F63695-DC97-4E8E-9FC6-412FDD4F4483
Q40981091-48F63695-DC97-4E8E-9FC6-412FDD4F4483
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Statement
http://www.wikidata.org/entity/statement/Q40981091-48F63695-DC97-4E8E-9FC6-412FDD4F4483
Isolated congenital hepatic fibrosis associated with TMEM67 mutations: report of a new genotype-phenotype relationship.
P2860
Q40981091-48F63695-DC97-4E8E-9FC6-412FDD4F4483
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40981091-48F63695-DC97-4E8E-9FC6-412FDD4F4483
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wasDerivedFrom
b425f5d75054865e1778f87ce108b08b5fc2a8d3
P2860
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).