000			02259 a2200661 4500
005			20250515041809.0
264		0	_c20061114
008			200611s 0 0 eng d
022			_a0364-5134
024	7		_a10.1002/ana.20963 _2doi
040			_aNLM _beng _cNLM
100	1		_aMukherjee, Odity
245	0	0	_aHDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin. _h[electronic resource]
260			_bAnnals of neurology _cSep 2006
300			_a314-22 p. _bdigital
500			_aPublication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; 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	_aAspartic Acid _xgenetics
650	0	4	_aChromosomes, Human, Pair 17
650	0	4	_aDNA Mutational Analysis _xmethods
650	0	4	_aDementia _xgenetics
650	0	4	_aFamily Health
650	0	4	_aFemale
650	0	4	_aGenetic Predisposition to Disease
650	0	4	_aHumans
650	0	4	_aImmunohistochemistry _xmethods
650	0	4	_aInclusion Bodies _xmetabolism
650	0	4	_aIntercellular Signaling Peptides and Proteins _xgenetics
650	0	4	_aMale
650	0	4	_aMiddle Aged
650	0	4	_aMutation, Missense
650	0	4	_aNeuropsychological Tests _xstatistics & numerical data
650	0	4	_aUbiquitin _xmetabolism
650	0	4	_aValine _xgenetics
650	0	4	_atau Proteins _xmetabolism
700	1		_aPastor, Pau
700	1		_aCairns, Nigel J
700	1		_aChakraverty, Sumi
700	1		_aKauwe, John S K
700	1		_aShears, Shantia
700	1		_aBehrens, Maria I
700	1		_aBudde, John
700	1		_aHinrichs, Anthony L
700	1		_aNorton, Joanne
700	1		_aLevitch, Denise
700	1		_aTaylor-Reinwald, Lisa
700	1		_aGitcho, Michael
700	1		_aTu, P-H
700	1		_aTenenholz Grinberg, Lea
700	1		_aLiscic, Rajka M
700	1		_aArmendariz, Javier
700	1		_aMorris, John C
700	1		_aGoate, Alison M
773	0		_tAnnals of neurology _gvol. 60 _gno. 3 _gp. 314-22
856	4	0	_uhttps://doi.org/10.1002/ana.20963 _zAvailable from publisher's website
999			_c16562603 _d16562603