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Q54977127-6350EF4C-20FD-49EC-AB4E-D51ADF6B9B40
Q54977127-6350EF4C-20FD-49EC-AB4E-D51ADF6B9B40
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-6350EF4C-20FD-49EC-AB4E-D51ADF6B9B40
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.
P1476
Q54977127-6350EF4C-20FD-49EC-AB4E-D51ADF6B9B40
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-6350EF4C-20FD-49EC-AB4E-D51ADF6B9B40
rank
NormalRank
type
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wasDerivedFrom
17f22ff4222e9d2c3e42a19883f83a8ffdd62255
P1476
A case report: a heterozygous
......
yopathies in a Chinese family.
@en