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S12883-018-1078-4
S12883-018-1078-4
http://dx.doi.org/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.
P356
Q54977127-AA81EE74-7CC3-4457-B0E8-CD60EBC3B101
P356
S12883-018-1078-4
http://dx.doi.org/10.1186/S12883-018-1078-4