000 01376 a2200385 4500
005 20250513200647.0
264 0 _c20000118
008 200001s 0 0 eng d
022 _a0893-0341
024 7 _a10.1097/00002093-199910000-00008
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKamimura, K
245 0 0 _aIdentification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
_h[electronic resource]
260 _bAlzheimer disease and associated disorders
_c
300 _a222-5 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aDementia, Multi-Infarct
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aJapan
650 0 4 _aMale
650 0 4 _aMembrane Proteins
_xgenetics
650 0 4 _aMutation, Missense
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPolymorphism, Single-Stranded Conformational
650 0 4 _aReceptors, Notch
700 1 _aTakahashi, K
700 1 _aUyama, E
700 1 _aTokunaga, M
700 1 _aKotorii, S
700 1 _aUchino, M
700 1 _aTabira, T
773 0 _tAlzheimer disease and associated disorders
_gvol. 13
_gno. 4
_gp. 222-5
856 4 0 _uhttps://doi.org/10.1097/00002093-199910000-00008
_zAvailable from publisher's website
999 _c10565646
_d10565646