Citations for
1HDL1, PRNP
Childhood onset in familial prion disease with a novel mutation in the PRNP gene.
1: Related Articles, LinksRogaeva E, Zadikoff C, Ponesse J, Schmitt-Ulms G, Kawarai T, Sato C, Salehi-Rad S, St George-Hyslop P, Lang AE.
Arch Neurol 63(7):1016-21. 2006
2HDL1, PRNP
Huntington disease phenocopy is a familial prion disease.
Moore RC, Xiang F, Monaghan J, Han D, Zhang Z, Edstrom L, Anvret M, Prusiner SB.
Am J Hum Genet 69(6):1385-8. Epub 2001 Oct 9. 2001
3GSSS, HDL1, PRNP
Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene.
Laplanche JL, Hachimi KH, Durieux I, Thuillet P, Defebvre L, Delasnerie-Laupretre N, Peoc'h K, Foncin JF, Destee A.
Brain 122 ( Pt 12):2375-86. 1999
4HDL1, PRNP
A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.
Xiang F, Almqvist EW, Huq M, Lundin A, Hayden MR, Edstrom L, Anvret M, Zhang Z.
Am J Hum Genet 63(5):1431-8. 1998