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Archives: Publication

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21

February 19, 2021

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

February 19, 2021

The origin of phenotypic heterogeneity in a clonal cell population in vitro

February 19, 2021

Age-Related Cataracts in {alpha}3Cx46-Knockout Mice Are Dependent on a Calpain 3 Isoform

February 19, 2021

A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay

February 19, 2021

Expression stochastique des gènes

February 19, 2021

Self-Promoted Cellular Uptake of Peptide/DNA Transfection Complexes

February 19, 2021

Current challenges in AAV systemic delivery in humans. in Virus Expression Vectors

February 19, 2021

Autologous transplantation of muscle precursor cells modified with a lentivirus for muscular dystrophy: human cells and primate models

February 19, 2021

The Nuclear Factor B–Activator Gene PLEKHG5 Is Mutated in a Form of Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

February 19, 2021

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