Research of Charcot-marie-tooth Disease has been linked to Muscular Atrophy, Peripheral Neuropathy, Hereditary Motor And Sensory Neuropathies, Atrophy, Sensory Neuropathy. The study of Charcot-marie-tooth Disease has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Charcot-marie-tooth Disease include Pathogenesis, Myelination, Localization, Transport, Muscle Atrophy. These pathways complement our catalog of research reagents for the study of Charcot-marie-tooth Disease including antibodies and ELISA kits against PMP22, MPZ, GJB1, PXMP2, KIF1B.
Charcot-marie-tooth Disease 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 Charcot-marie-tooth Disease below!
For more information on how to use Laverne, please read the How to Guide.
We have 1049 products for the study of Charcot-marie-tooth Disease that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Charcot-marie-tooth Disease is also known as charcot-marie-tooth disease, cmt, pma, charcot-marie-tooth hereditary neuropathy, hereditary motor and sensory neuropathies, peroneal muscular atrophy nos (disorder), charcot-marie-tooth disease (disorder), charcot marie tooth muscular atrophy, dejerine-sottas disease (disorder), cmt - charcot-marie-tooth disease, roussy-levy syndrome (disorder), charcot marie tooth disease, dejerine-sottas syndrome, roussy-levy syndrome.
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