FLNC-Associated Myofibrillar Myopathy
Por um escritor misterioso
Descrição
Cells, Free Full-Text
A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.
Analysis of a putative second dimerization region in FLNc. a
Myofibrillar Myopathies: New Perspectives from Animal Models to Potential Therapeutic Approaches - IOS Press
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood, Orphanet Journal of Rare Diseases
FLNC-Associated Myofibrillar Myopathy
Filamin C regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy - ScienceDirect
Myofibrillar myopathy: MedlinePlus Genetics
Filamin C regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy - ScienceDirect
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