Genetic diseases of muscle.

Abstract excerpt

In the last twenty years, the genetic basis for most of the inherited myopathies and muscular dystrophies has been unveiled. Diseases have been found to result from loss of function of structural components of the muscle basal lamina (e.g., MCD1A), sarcolemma (e.g., the sarcoglycanopathies), nucleus (e.g., EDMD) and sarcomere (e.g., the nemaline myopathies). A few have been associated with abnormalities in the...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Genetic Markers
• Share to Genetic Testing
• Share to Genotype