Research of Juvenile Spinal Muscular Atrophy has been linked to Muscular Atrophy, Atrophy, Spinal Muscular Atrophy, Spinal Muscular Atrophies Of Childhood, Weakness. The study of Juvenile Spinal Muscular Atrophy has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Juvenile Spinal Muscular Atrophy include Pathogenesis, Muscle Atrophy, Innervation, Collateral Sprouting, Cell Adhesion. These pathways complement our catalog of research reagents for the study of Juvenile Spinal Muscular Atrophy including antibodies and ELISA kits against HEXOSAMINIDASE A, SURVIVAL MOTOR NEURON 1, THYROTROPIN RELEASING HORMONE, C5, C7.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Juvenile Spinal Muscular Atrophy below!
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We have 502 products for the study of Juvenile Spinal Muscular Atrophy that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Juvenile Spinal Muscular Atrophy is also known as juvenile spinal muscular atrophy, kugelberg-welander disease, sma3, spinal muscular atrophy, mild childhood and adolescent form, spinal muscular atrophy of childhood, spinal muscular atrophy, familial, type iii spinal muscular atrophy, spinal muscular atrophy type 3, kugelberg-welander syndrome, muscular atrophy, juvenile, spinal muscular atrophy-3, spinal muscular atrophy, sma iii, sma 3, kws.