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Q54977127-434F5D16-1ECF-44F0-98C7-7725174605DF
Q54977127-434F5D16-1ECF-44F0-98C7-7725174605DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-434F5D16-1ECF-44F0-98C7-7725174605DF
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.
P1433
Q54977127-434F5D16-1ECF-44F0-98C7-7725174605DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-434F5D16-1ECF-44F0-98C7-7725174605DF
rank
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type
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wasDerivedFrom
17f22ff4222e9d2c3e42a19883f83a8ffdd62255
P1433
BMC Neurology