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: | Allamand Valérie, Briñas Laura, Richard Pascale, Stojkovic Tanya, Quijano-Roy Susana, Bonne Gisèle |
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Format: | Article |
Language: | English |
Published: |
BMC
2011-09-01
|
Series: | Skeletal Muscle |
Online Access: | http://www.skeletalmusclejournal.com/content/1/1/30 |
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