Muscular Dystrophy, Limb-girdle, Type 2d: Disease Bioinformatics
Limb-girdle muscular dystrophy type 2d is a rare disorder that results in muscles weakness and atrophy. Mutations in the SGCA gene cause limb-girdle muscular dystrophy type 2d, which is inherited in an autosomal recessive pattern. Symptoms of limb-girdle muscular dystrophy type 2d appear in earlier childhood and worsen as time progresses. Limb-girdle muscular dystrophy primarily causes weakness in proximal muscles, which makes walking difficult and can be disabling. In some cases, the heart and lung muscles also weaken, causing difficulty in breathing. Currently, there is no cure for limb-girdle muscular dystrophy type 2d, and treatment for the disorder is supportive.
Muscular Dystrophy, Limb-girdle, Type 2d 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 Muscular Dystrophy, Limb-girdle, Type 2d below!
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We have 265 products for the study of Muscular Dystrophy, Limb-girdle, Type 2d that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.