Polymorphism at 3′ UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt–Jakob disease-Reference-Cited by-同舟云学术

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Polymorphism at 3′ UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt–Jakob disease

Published:2005-06-29 Issue:9 Volume:13 Page:1094-1097
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Jeong Byung-Hoon,Kim Nam-Ho,Choi Eun-Kyoung,Lee Chaeyoung,Song Young-Han,Kim Jae-Il,Carp Richard I,Kim Yong-Sun

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201460.pdf

Reference24 articles.

1. Prusiner SB : Introduction: prion diseases. Sem Virol 1996; 7: 157–173.

2. Doh-ura K, Tateishi J, Sasaki H, Kitamoto T, Sakaki Y : Pro → leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann–Sträussler syndrome. Biochem Biophys Res Commun 1989; 163: 974–979.

3. Goldfarb LG, Brown P, McCombie WR et al: Transmissible familial Creutzfeldt–Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. Proc Natl Acad Sci USA 1991; 88: 10926–10930.

4. Medori R, Montagna P, Tritschler HJ et al: Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178. Neurology 1992; 42: 669–670.

5. Collinge J, Palmer MS, Dryden AJ : Genetic predisposition to iatrogenic Creutzfeldt–Jakob disease. Lancet 1991; 337: 1411–1442.

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3. Identification of the prion-related protein gene (PRNT) sequences in various species of the Cervidae family;Molecular Biology Reports;2020-07-31

4. Genetic characteristics and polymorphisms in the chicken interferon-induced transmembrane protein (IFITM3) gene;Veterinary Research Communications;2019-08-13

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