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What Should the Cardiologist know about Lamin Disease? | AER Journal
What Should the Cardiologist know about Lamin Disease? | AER Journal

A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS

Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics

CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy

Hutchinson-Gilford progeria patient-derived cardiomyocyte model of carrying LMNA gene variant c.1824 C > T | SpringerLink
Hutchinson-Gilford progeria patient-derived cardiomyocyte model of carrying LMNA gene variant c.1824 C > T | SpringerLink

Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics

Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy: Molecular Therapy - Nucleic Acids
Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy: Molecular Therapy - Nucleic Acids

Prelamin-A/C - Wikipedia
Prelamin-A/C - Wikipedia

Schematic representation of MADA pathogenic mutations in LMNA gene... | Download Scientific Diagram
Schematic representation of MADA pathogenic mutations in LMNA gene... | Download Scientific Diagram

p.Pro4Arg mutation in LMNA gene: a new atypical progeria phenotype without metabolism abnormalities - ScienceDirect
p.Pro4Arg mutation in LMNA gene: a new atypical progeria phenotype without metabolism abnormalities - ScienceDirect

A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy | Human Genome Variation
A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy | Human Genome Variation

LMNA » Laboratory Testing and Research
LMNA » Laboratory Testing and Research

LMNA Protein Overview: Sequence, Structure, Function and Protein Interaction | Sino Biological
LMNA Protein Overview: Sequence, Structure, Function and Protein Interaction | Sino Biological

LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody
LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody

Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype

Genes | Free Full-Text | LMNA Mutations G232E and R482L Cause Dysregulation of Skeletal Muscle Differentiation, Bioenergetics, and Metabolic Gene Expression Profile
Genes | Free Full-Text | LMNA Mutations G232E and R482L Cause Dysregulation of Skeletal Muscle Differentiation, Bioenergetics, and Metabolic Gene Expression Profile

LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody
LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody

The LMNA gene and its putative association with human ageing
The LMNA gene and its putative association with human ageing

LMNA - an overview | ScienceDirect Topics
LMNA - an overview | ScienceDirect Topics

Normal and aberrant splicing of LMNA | Journal of Medical Genetics
Normal and aberrant splicing of LMNA | Journal of Medical Genetics

LMNA Mutations Associated With Mild and Late-Onset Phenotype | Circulation: Cardiovascular Genetics
LMNA Mutations Associated With Mild and Late-Onset Phenotype | Circulation: Cardiovascular Genetics

PDF] LMNA cardiomyopathy: cell biology and genetics meet clinical medicine | Semantic Scholar
PDF] LMNA cardiomyopathy: cell biology and genetics meet clinical medicine | Semantic Scholar

Schematic of the LMNA gene and lamin A protein indicating... | Download Scientific Diagram
Schematic of the LMNA gene and lamin A protein indicating... | Download Scientific Diagram

LMNA Gene Amplification Kit for direct sequencing - Diatheva
LMNA Gene Amplification Kit for direct sequencing - Diatheva

What Should the Cardiologist know about Lamin Disease? | AER Journal
What Should the Cardiologist know about Lamin Disease? | AER Journal

Frontiers | Exploring the Crosstalk Between LMNA and Splicing Machinery Gene Mutations in Dilated Cardiomyopathy
Frontiers | Exploring the Crosstalk Between LMNA and Splicing Machinery Gene Mutations in Dilated Cardiomyopathy

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
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

Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease | PLOS ONE
Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease | PLOS ONE