000 01654 a2200493 4500
005 20250515020527.0
264 0 _c20060425
008 200604s 0 0 eng d
022 _a0003-9942
024 7 _a10.1001/archneur.63.3.449
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBasset-Leobon, Céline
245 0 0 _aFamilial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques.
_h[electronic resource]
260 _bArchives of neurology
_cMar 2006
300 _a449-52 p.
_bdigital
500 _aPublication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAmyloid
_xgenetics
650 0 4 _aArginine
_xgenetics
650 0 4 _aBlotting, Western
_xmethods
650 0 4 _aBrain
_xpathology
650 0 4 _aCreutzfeldt-Jakob Syndrome
_xgenetics
650 0 4 _aHaplotypes
650 0 4 _aHistidine
_xgenetics
650 0 4 _aHumans
650 0 4 _aImmunohistochemistry
_xmethods
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aPlaque, Amyloid
_xpathology
650 0 4 _aPrion Proteins
650 0 4 _aPrions
650 0 4 _aProtein Precursors
_xgenetics
650 0 4 _aValine
_xgenetics
700 1 _aUro-Coste, Emmanuelle
700 1 _aPeoc'h, Katell
700 1 _aHaik, Stéphane
700 1 _aSazdovitch, Véronique
700 1 _aRigal, Mathieu
700 1 _aAndreoletti, Olivier
700 1 _aHauw, Jean-Jacques
700 1 _aDelisle, Marie-Bernadette
773 0 _tArchives of neurology
_gvol. 63
_gno. 3
_gp. 449-52
856 4 0 _uhttps://doi.org/10.1001/archneur.63.3.449
_zAvailable from publisher's website
999 _c16142943
_d16142943