FLNC-Associated Myofibrillar Myopathy
Por um escritor misterioso
Descrição
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood, Orphanet Journal of Rare Diseases
Filamin C regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy - ScienceDirect
P3 Allele of FLNC is Associated with Myofibrillar Myopathy in Horses – Equiseq
Structure of the FLNC gene and filamin C protein. (a) Within the human
A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report, BMC Neurology
A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report, BMC Neurology
Cureus, DES c.1360C>T: A Rare Desmin Variant Causing Early Distal Myopathy and Cardiomyopathy
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
Filamin C regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy - ScienceDirect
Myofibrillar myopathy: MedlinePlus Genetics
