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Q41055576-87A4B19D-04AA-4942-8023-8D7C654009CA
Q41055576-87A4B19D-04AA-4942-8023-8D7C654009CA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41055576-87A4B19D-04AA-4942-8023-8D7C654009CA
Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita.
P1476
Q41055576-87A4B19D-04AA-4942-8023-8D7C654009CA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41055576-87A4B19D-04AA-4942-8023-8D7C654009CA
rank
NormalRank
type
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Statement
wasDerivedFrom
66d7b7288677e449ec7267fd38581ec867e9e73b
P1476
Expanding the MYBPC1 phenotypi
......
ogryposis multiplex congenita.
@en