(Q36374006)
Statements
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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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16
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2
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113-121
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Identifiers
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1 reference