RNF213 Polymorphisms in Intracranial Artery Dissection
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Clinical Spectrum of CADASIL:A Study of 7 Families
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
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