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Novel Filamin C (FLNC) Variant Causes a Severe Form of Familial Mixed Hypertrophic-Restrictive Cardiomyopathy

Novel filamin C (FLNC) variant causes a severe form of familial mixed hypertrophic-restrictive cardiomyopathy

Authors: Gaudreault N, Ruel LJ, Henry C, Schleit J, Lagüe P, Champagne J, Sénéchal M, Sarrazin JF, Philippon F, Bossé Y, Steinberg C

Am J Med Genet A. 2023 Mar 2. doi: 10.1002/ajmg.a.63169. Online ahead of print.

Disclaimer: One or more of the authors of this publication were employed at the time by BluePrint Genetics, a subsidiary of Quest Diagnostics.

Specialties: Genetics, Oncology

 

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