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Q54977127-9C641FB2-8D7C-4FFF-ADF7-8B1E8DA7D0C3
Q54977127-9C641FB2-8D7C-4FFF-ADF7-8B1E8DA7D0C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-9C641FB2-8D7C-4FFF-ADF7-8B1E8DA7D0C3
A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.
P577
Q54977127-9C641FB2-8D7C-4FFF-ADF7-8B1E8DA7D0C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-9C641FB2-8D7C-4FFF-ADF7-8B1E8DA7D0C3
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
17f22ff4222e9d2c3e42a19883f83a8ffdd62255
P577
2018-06-04T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P577
41c3b51a634b78e7cde6229cc5c80fa8