Spinal Muscular Atrophy
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Molecular Genetics in Neurology
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Adrenoleukodystrophy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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Clinical Spectrum of CADASIL:A Study of 7 Families
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
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Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
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