Genetic prion disease: D178N with 129MV disease modifying polymorphism—a clinical phenotype | BMJ Neurology Open

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Genetic prion disease: D178N with 129MV disease modifying polymorphism—a clinical phenotype

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Cite this article as:: Tan TH, Stark RJ, Waterston JA, et al

Genetic prion disease: D178N with 129MV disease modifying polymorphism—a clinical phenotype

BMJ Neurology Open 2020;2:e000074. doi: 10.1136/bmjno-2020-000074