000 01773 a2200553 4500
005 20250513193949.0
264 0 _c20000204
008 200002s 0 0 eng d
022 _a0304-3940
024 7 _a10.1016/s0304-3940(99)00669-2
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBonifati, V
245 0 0 _aThe tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases.
_h[electronic resource]
260 _bNeuroscience letters
_cOct 1999
300 _a61-5 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAged
650 0 4 _aAlleles
650 0 4 _aDNA Mutational Analysis
650 0 4 _aExons
_xgenetics
650 0 4 _aHaplotypes
650 0 4 _aHumans
650 0 4 _aIntrons
_xgenetics
650 0 4 _aItaly
650 0 4 _aMutation
_xgenetics
650 0 4 _aProtein Isoforms
650 0 4 _aRNA Splicing
_xgenetics
650 0 4 _aSupranuclear Palsy, Progressive
_xgenetics
650 0 4 _atau Proteins
_xgenetics
700 1 _aJoosse, M
700 1 _aNicholl, D J
700 1 _aVanacore, N
700 1 _aBennett, P
700 1 _aRizzu, P
700 1 _aFabbrini, G
700 1 _aMarconi, R
700 1 _aColosimo, C
700 1 _aLocuratolo, N
700 1 _aStocchi, F
700 1 _aBonuccelli, U
700 1 _aDe Mari, M
700 1 _aWenning, G
700 1 _aVieregge, P
700 1 _aOostra, B
700 1 _aMeco, G
700 1 _aHeutink, P
773 0 _tNeuroscience letters
_gvol. 274
_gno. 1
_gp. 61-5
856 4 0 _uhttps://doi.org/10.1016/s0304-3940(99)00669-2
_zAvailable from publisher's website
999 _c10487436
_d10487436