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FLNC-Associated Myofibrillar Myopathy

Por um escritor misterioso
Last updated 05 abril 2025
FLNC-Associated Myofibrillar Myopathy
FLNC-Associated Myofibrillar Myopathy
Myofibrillar myopathy: MedlinePlus Genetics
FLNC-Associated Myofibrillar Myopathy
Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy - Cui - 2018 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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
PDF) FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic Data
FLNC-Associated Myofibrillar Myopathy
Analysis of a putative second dimerization region in FLNc. a
FLNC-Associated Myofibrillar Myopathy
Muscles, Free Full-Text
FLNC-Associated Myofibrillar Myopathy
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation
FLNC-Associated Myofibrillar Myopathy
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation
FLNC-Associated Myofibrillar Myopathy
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy
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