FLNC-Associated Myofibrillar Myopathy
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Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation, Acta Neuropathologica Communications
FLNC-Associated Myofibrillar Myopathy
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation
FLNC-Associated Myofibrillar Myopathy
Cells, Free Full-Text
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood, Orphanet Journal of Rare Diseases
Frontiers Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center
Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation, Acta Neuropathologica Communications
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
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