ColVI myopathies: where do we stand, where do we go?
<p>Abstract</p> <p>Collagen VI myopathies, caused by mutations in the genes encoding collagen type VI (ColVI), represent a clinical continuum with Ullrich congenital muscular dystrophy (UCMD) and Bethlem myopathy (BM) at each end of the spectrum, and less well-defined intermediate...
| Main Authors: | , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
BMC
2011-09-01
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| Series: | Skeletal Muscle |
| Online Access: | http://www.skeletalmusclejournal.com/content/1/1/30 |