Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred (Q36374006)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred |
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Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred (English)
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David O Hutchinson
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Amanda Charlton
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Biljana Ilkovski
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19 January 2006
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