FLNC-Associated Myofibrillar Myopathy
Por um escritor misterioso
Descrição
![FLNC-Associated Myofibrillar Myopathy](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs40478-020-01001-9/MediaObjects/40478_2020_1001_Fig3_HTML.png)
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](https://www.neurology.org/cms/10.1212/NXG.0000000000000590/asset/34529788-e943-4720-a529-284687197769/assets/graphic/nxg.0000000000000590f3.jpeg)
FLNC-Associated Myofibrillar Myopathy
![FLNC-Associated Myofibrillar Myopathy](https://www.ahajournals.org/cms/asset/84e0a376-d809-4875-aa85-bcfa663a2102/circresaha.120.317076.fig03.jpg)
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation
![FLNC-Associated Myofibrillar Myopathy](https://www.neurology.org/cms/asset/4b89bd2a-ec8b-4619-b6b8-36f669b4e40e/nxg.2021.7.issue-3.largecover.jpg)
FLNC-Associated Myofibrillar Myopathy
![FLNC-Associated Myofibrillar Myopathy](https://pub.mdpi-res.com/cells/cells-12-01321/article_deploy/html/images/cells-12-01321-g009.png?1683282883)
Cells, Free Full-Text
![FLNC-Associated Myofibrillar Myopathy](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs13023-022-02477-5/MediaObjects/13023_2022_2477_Fig2_HTML.jpg)
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood, Orphanet Journal of Rare Diseases
![FLNC-Associated Myofibrillar Myopathy](https://www.frontiersin.org/files/Articles/533769/fneur-11-01014-HTML-r1/image_m/fneur-11-01014-g002.jpg)
Frontiers Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center
![FLNC-Associated Myofibrillar Myopathy](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs40478-020-01001-9/MediaObjects/40478_2020_1001_Fig4_HTML.png)
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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fncomms6326/MediaObjects/41467_2014_Article_BFncomms6326_Fig4_HTML.jpg)
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
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