Codon 200 mutation of the prion gene: genotype–phenotype correlations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/content/pdf/10.1007/s00415-012-6539-x.pdf
Reference25 articles.
1. Mead S (2006) Prion disease genetics. Euro J Hum Genet 14:273–281
2. Mastrianni JA (2010) The genetics of prion diseases. Genet Med 12:187–195
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4. Heinemann U, Krasniansi A, Meissner B, Varges D, Kallenberg K, Schulz-Schaeffer WJ et al (2007) Creutzfeldt–Jakob disease in Germany: a prospective 12-year surveillance. Brain 130:1350–1359
5. Schmitz M, Schlomm M, Hasan B, Beekes M, Mitrova E, Korth C et al (2010) Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt–Jakob disease. Euro J Neurosci 31:2024–2031
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