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Settore MED/26 - Neurologia
AGL gene
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Myotonic dystrophy type 1
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RNA processing
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amylo-1,6-glucosidase
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cognitive disturbance
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cross-cultural assessment
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founder effect
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glycogen storage disease type III
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haplotype analysi
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migration
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myotonic dystrophy type 2
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novel mutation
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public health
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skeletal muscle
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