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Amedeo Smart

Independent Medical Education


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Zhang J, Chen MJ, Zhao GX, Li HF, et al. Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population. J Neurol 2020 Aug 29. pii: 10.1007/s00415-020-10184.
PMID: 32862241


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