Nemaline Myopathy 10

About the Disease
Nemaline Myopathy 10, also known as nem10, is related to myopathy and locked-in syndrome, and has symptoms including ophthalmoplegia, facial paresis and generalized muscle weakness. An important gene associated with Nemaline Myopathy 10 is LMOD3 (Leiomodin 3). Affiliated tissues include skeletal muscle, and related phenotypes are facial palsy and skeletal muscle atrophy

Common Targets
LMOD3

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