LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody
What Should the Cardiologist know about Lamin Disease? | AER Journal
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
Prelamin-A/C - Wikipedia
Frontiers | Genomic analysis of a novel pathogenic variant in the gene LMNA associated with cardiac laminopathies found in Ecuadorian siblings: A case report
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
Schematic of the LMNA gene and lamin A protein indicating... | Download Scientific Diagram
What Should the Cardiologist know about Lamin Disease? | AER Journal
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics
Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease | PLOS ONE
LMNA - an overview | ScienceDirect Topics
LMNA » Laboratory Testing and Research
Modulation of cytoskeleton in cardiomyopathy caused by mutations in LMNA gene | American Journal of Physiology-Cell Physiology
Frontiers | Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights
The role of genetic mutations in genes LMNA, PPARG, PLIN1, AKT2, CIDEC in Köbberling–Dunnigan Syndrome
Schematic representation of MADA pathogenic mutations in LMNA gene... | Download Scientific Diagram
LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody
LMNA mutations detected in patients. (A) Representation of mutations... | Download Scientific Diagram
Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and ex vivo studies - Figure f3 | Aging
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
Deletion of the Lmna gene in fibroblasts causes senescence-associated dilated cardiomyopathy by activating the double-stranded DNA damage response and induction of senescence-associated secretory phenotype
Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy: Molecular Therapy - Nucleic Acids
Generation of Lamin A/C gene (Lmna) exon 4 mutations using CRISPR/Cas... | Download Scientific Diagram
LMNA Gene Amplification Kit for direct sequencing - Diatheva
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy
Normal and aberrant splicing of LMNA | Journal of Medical Genetics
