Associated Papers
Whole-exome sequencing to identify causative variants in juvenile sudden cardiac death.
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Human Genomics, 2024
LMNA-associated myopathies: the Italian experience in a large cohort of patients.
Maggi L et al.
Neurology, 2014
Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature.
Captur G et al.
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30402260 (PubMed )
Supplement: openhrt-2018-000915supp002.xlsx › gnomad_ENSG00000160789_2017_12_
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