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Bethlem myopathy
A usually autosomal dominant inherited movement disorder caused by mutations in the COL6A1, COL6A2, and COL6A3 genes. It is characterized by progressive muscle weakness and joint stiffness in the fingers, wrists, elbows, and ankles.
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Bethlem myopathy 1A 0 trials
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Bethlem myopathy 1B 0 trials
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Bethlem myopathy 1C 0 trials
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Bethlem myopathy 2 0 trials