FLNC-Associated Myofibrillar Myopathy
Por um escritor misterioso
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Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
Expanding the central nervous system disease spectrum associated with FLNC mutation - Previtali - 2019 - Muscle & Nerve - Wiley Online Library
A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report, BMC Neurology
Cells, Free Full-Text
Muscles, Free Full-Text
Cells, Free Full-Text
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy
Myofibrillar myopathy: MedlinePlus Genetics
Muscles, Free Full-Text
FLNC-Associated Myofibrillar Myopathy
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
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