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Q54977127-DA4FFD61-37F1-47CD-A068-8AA47771A4D3
Q54977127-DA4FFD61-37F1-47CD-A068-8AA47771A4D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-DA4FFD61-37F1-47CD-A068-8AA47771A4D3
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.
P6179
Q54977127-DA4FFD61-37F1-47CD-A068-8AA47771A4D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-DA4FFD61-37F1-47CD-A068-8AA47771A4D3
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
95c9cf03a69e929022cd2f0e678d78ac864c1afb
P6179
1104385384
http://www.w3.org/2001/XMLSchema#string