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Predominant Spastic Paraparesis Associated With the D178N Mutation in PRNP

Sebastian Thams1, Martin Paucar1, Louise Wingård1

  • 1Department of Neurology (S.T., M.P., P.S.), Karolinska University Hospital, Stockholm, Sweden; Department of Clinical Neuroscience (S.T., M.P., P.S.), Karolinska Institutet, Stockholm, Sweden; Department of Psychiatry (L.W.), North West District in Stockholm, Sweden; Department of Molecular Medicine and Surgery (H.T.), Center for Molecular Medicine, Karolinska Institutet; Department of Clinical Genetics (H.T.), Karolinska University Laboratory, Karolinska University Hospital; Colin Smith (C.S.), National CJD Research & Surveillance Unit, Edinburgh, United Kingdom; and Department of Pathology (I.N.), Karolinska University Hospital, Stockholm, Sweden.

Neurology. Genetics
|November 8, 2021
PubMed
Abstract

No abstract available in PubMed .

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