anticodon and Wallerian-Degeneration

anticodon has been researched along with Wallerian-Degeneration* in 1 studies

Other Studies

1 other study(ies) available for anticodon and Wallerian-Degeneration

ArticleYear
Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene.
    Neurology, 2006, Nov-14, Volume: 67, Issue:9

    We screened 100 patients with inherited and sporadic lower motor neuron degeneration and identified three novel missense mutations in the glycyl-tRNA synthetase (GARS) gene. One mutation was in the anticodon binding domain and associated with onset in early childhood and predominant involvement of the lower limbs, thus extending the phenotype associated with GARS mutations.

    Topics: Adult; Aged, 80 and over; Anticodon; Axons; Binding Sites; Charcot-Marie-Tooth Disease; Child; Cohort Studies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Glycine-tRNA Ligase; Humans; Male; Motor Neurons; Muscle, Skeletal; Mutation; Protein Biosynthesis; Protein Structure, Tertiary; Spinal Muscular Atrophies of Childhood; Wallerian Degeneration

2006