TY - JOUR AU - Chen, Juanjuan AU - Wu, Jun AU - Han, Chunxi AU - Li, Yao AU - Guo, Yuzu AU - Tong, Xiaoxin PY - 2019 DA - 2019/08/17 TI - A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report JO - BMC Neurology SP - 198 VL - 19 IS - 1 AB - Myofibrillar myopathies (MFMs) are a genetically heterogeneous group of muscle disorders. Mutations in the filamin C gene (FLNC) have previously been identified in patients with MFM. The phenotypes of FLNC-related MFM are heterogeneous. SN - 1471-2377 UR - https://doi.org/10.1186/s12883-019-1410-7 DO - 10.1186/s12883-019-1410-7 ID - Chen2019 ER -