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De Novo Mutation in the Notch3 Gene Causing CADASIL
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NEJM 360:1656-1665, Case 12-2009, 2009
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Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005
Retinocochleocerebral Vasculopathy
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997
Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
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