Research of Spinal Muscular Atrophy has been linked to Muscular Atrophy, Atrophy, Spinal Muscular Atrophies Of Childhood, Neuromuscular Diseases, Weakness. The study of Spinal Muscular Atrophy has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Spinal Muscular Atrophy include Pathogenesis, Muscle Atrophy, Localization, Transport, Cell Death. These pathways complement our catalog of research reagents for the study of Spinal Muscular Atrophy including antibodies and ELISA kits against SMN2, SMN1, SNRPN, STMN1, AR.
Spinal Muscular Atrophy Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Spinal Muscular Atrophy below!
For more information on how to use Laverne, please read the How to Guide.
We have 893 products for the study of Spinal Muscular Atrophy that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunohistochemistry, Immunocytochemistry/Immunofluorescence from our catalog of antibodies and ELISA kits.
Spinal Muscular Atrophy is also known as spinal muscular atrophy, progressive muscular atrophy, sma, hereditary motor neuronopathy, muscular atrophy spinal, muscular atrophy, smn.
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