000 01385 a2200409 4500
005 20250513051455.0
264 0 _c19940823
008 199408s 0 0 eng d
022 _a0962-8436
024 7 _a10.1098/rstb.1994.0034
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKitamoto, T
245 0 0 _aHuman prion diseases with variant prion protein.
_h[electronic resource]
260 _bPhilosophical transactions of the Royal Society of London. Series B, Biological sciences
_cMar 1994
300 _a391-8 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aAged, 80 and over
650 0 4 _aAmino Acid Sequence
650 0 4 _aBase Sequence
650 0 4 _aCodon
_xgenetics
650 0 4 _aDNA Primers
_xgenetics
650 0 4 _aGenetic Variation
650 0 4 _aHumans
650 0 4 _aJapan
650 0 4 _aMiddle Aged
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aPrPSc Proteins
650 0 4 _aPrion Diseases
_xgenetics
650 0 4 _aPrions
_xgenetics
700 1 _aTateishi, J
773 0 _tPhilosophical transactions of the Royal Society of London. Series B, Biological sciences
_gvol. 343
_gno. 1306
_gp. 391-8
856 4 0 _uhttps://doi.org/10.1098/rstb.1994.0034
_zAvailable from publisher's website
999 _c7913090
_d7913090