Associated Papers
The Definition of Sarcomeric and Non-Sarcomeric Gene Mutations in Hypertrophic Cardiomyopathy Patients: A Multicenter Diagnostic Study Across Türkiye.
Oktay V et al.
Anatolian Journal of Cardiology, 2023
Filamin C in cardiomyopathy: from physiological roles to DNA variants.
Song S et al.
Heart Failure Reviews, 2022
Clinical exome sequencing revealed that FLNC variants contribute to the early diagnosis of cardiomyopathies in infant patients.
Xiao F et al.
Translational Pediatrics, 2020
Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service.
Westra D et al.
Journal of Neuromuscular Diseases, 2019
31127727 (PubMed )
Supplement: sj-xlsx-2-jnd-10.3233_jnd-180376.xlsx › Blad1
Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy.
Cui H et al.
Molecular Genetics & Genomic Medicine, 2018
The genomic complexity of primary human prostate cancer.
Berger MF et al.
Nature, 2011
21307934 (PubMed )
Supplement: NIHMS257464-supplement-2.xlsx › TABLE_S3
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