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Advances in the Genetics of Cerebrovascular Disease and Stroke
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Huntington Disease: Clinical Features and Diagnosis
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Neurofibromatosis Type 2
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
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Clinical Genetics in Neurological Disease
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Detecting Susceptibility to Malignant Hyperthermia
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Cockayne Syndrome: Review of 140 Cases
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