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Q54977127-3A220AAC-6E93-43CB-9183-DD737D807D88
Q54977127-3A220AAC-6E93-43CB-9183-DD737D807D88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-3A220AAC-6E93-43CB-9183-DD737D807D88
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.
P932
Q54977127-3A220AAC-6E93-43CB-9183-DD737D807D88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-3A220AAC-6E93-43CB-9183-DD737D807D88
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
17f22ff4222e9d2c3e42a19883f83a8ffdd62255
P932
5985593
http://www.w3.org/2001/XMLSchema#string