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myopathy, spheroid body
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MYOT
Myotilin dynamics in cardiac and skeletal muscle cells
Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q
The gene for Treacher Collins syndrome maps to the long arm of chromosome 5
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31
Cancer Gene Census
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