Exploring Splice-Site Mutations in LAMA2-Related Muscular Dystrophies: A Comprehensive Analysis of Genotypic and Phenotypic Patterns. [PDF]
Nmer S +5 more
europepmc +1 more source
The Interaction of LAMA2 and Duration of Illness Affects the Thickness of the Right Transverse Temporal Gyrus in Major Depressive Disorder. [PDF]
Chen G +10 more
europepmc +1 more source
A Prospective Study on the Feasibility and Effect of an Optimized Perioperative Care Protocol in Pediatric Neuromuscular Scoliosis Surgery. [PDF]
Naume MM +12 more
europepmc +1 more source
CRISPR-based Transcriptional Regulation: Technologies, Applications, and Future Directions. [PDF]
Srinivasa MA, Escobar M.
europepmc +1 more source
A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy. [PDF]
Nejati P +6 more
europepmc +1 more source
Identification of LAMA2 compound heterozygous variants: a case report. [PDF]
Ying Y, Ye J, Shen J, Chen G, Jiang K.
europepmc +1 more source
Autophagy in striated muscle diseases. [PDF]
Li H, Zhang L, Zhang L, Han R.
europepmc +1 more source
Emerging roles of microRNAs and other non-coding transcriptome in muscular dystrophies. [PDF]
Abdelrehim FG +5 more
europepmc +1 more source
A Spectrum of Pathogenic Variants in the <i>LAMA2</i> Gene in the Russian Federation. [PDF]
Chausova P +22 more
europepmc +1 more source

