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Q41055576-F4ACC8E2-FAA0-485E-92AD-69A9D6D4BA88
Q41055576-F4ACC8E2-FAA0-485E-92AD-69A9D6D4BA88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41055576-F4ACC8E2-FAA0-485E-92AD-69A9D6D4BA88
Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita.
P356
Q41055576-F4ACC8E2-FAA0-485E-92AD-69A9D6D4BA88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41055576-F4ACC8E2-FAA0-485E-92AD-69A9D6D4BA88
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
66d7b7288677e449ec7267fd38581ec867e9e73b
P356
10.1111/CGE.12707
http://www.w3.org/2001/XMLSchema#string
P356
CGE.12707