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Q54977127-A3220337-2437-4491-8CA4-9420575A05DA
Q54977127-A3220337-2437-4491-8CA4-9420575A05DA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-A3220337-2437-4491-8CA4-9420575A05DA
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.
P2888
Q54977127-A3220337-2437-4491-8CA4-9420575A05DA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-A3220337-2437-4491-8CA4-9420575A05DA
rank
NormalRank
type
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Statement
P2888
s12883-018-1078-4