Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy: Molecular Therapy - Nucleic Acids
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
Mechanisms of allelic and clinical heterogeneity of lamin A/C phenotypes | Physiological Genomics
Progeria
Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation | PLOS ONE
Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease | PLOS ONE
LMNA mutations detected in patients. (A) Representation of mutations... | Download Scientific Diagram
The UMD-LMNA database: the gene
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics
LMNA mutations in progeria patients. The diagram shows the structure of... | Download Scientific Diagram
Amelioration of desmin network defects by αB-crystallin overexpression confers cardioprotection in a mouse model of dilated cardiomyopathy caused by LMNA gene mutation - ScienceDirect
What Should the Cardiologist know about Lamin Disease? | AER Journal
Structural basis for lamin assembly at the molecular level | Nature Communications
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy
LMNA - an overview | ScienceDirect Topics
David R. Liu on Twitter: "The mutation (discovered by @NIHDirector's lab in 2003) results in progerin, a toxic protein that damages nuclei. So providing more healthy LMNA is not a solution, and
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
Uncategorized – Developmental Biology Research Highlights, University of Otago, New Zealand
Schematic representation of MADA pathogenic mutations in LMNA gene... | Download Scientific Diagram
Cells | Free Full-Text | Consequences of Lmna Exon 4 Mutations in Myoblast Function
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
Spectrum of LMNA mutations: schematic representation of LMNA mutations... | Download Scientific Diagram
Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease | NEJM
A novel lamin A/C gene mutation causing spinal muscular atrophy phenotype with cardiac involvement: report of one case | BMC Neurology | Full Text
