A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report

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-relate...
Source: BMC Neurology - Category: Neurology Authors: Tags: Case report Source Type: research