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s12883-018-1078-4
s12883-018-1078-4
https://scigraph.springernature.com/pub.10.1186/s12883-018-1078-4
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
95c9cf03a69e929022cd2f0e678d78ac864c1afb
P854
Q54977127-A3220337-2437-4491-8CA4-9420575A05DA
P2888
s12883-018-1078-4
https://scigraph.springernature.com/pub.10.1186/s12883-018-1078-4