Article

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

2019-08-06

Abstract excerpt

<title>Abstract</title> <p>Abstract Background: 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. Case presentation: The patient was a 37-year-old male who first experienced weakness in the distal muscles of his hand, which event...

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Literature Corpus work: afe5b526-5a49-5ece-b7d2-71d6ca4ff8ae
DOI: 10.21203/rs.2.348/v4

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