000 01454 a2200421 4500
005 20250516094351.0
264 0 _c20130212
008 201302s 0 0 eng d
022 _a1878-5883
024 7 _a10.1016/j.jns.2012.05.025
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTesti, S
245 0 0 _aMutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
_h[electronic resource]
260 _bJournal of the neurological sciences
_cAug 2012
300 _a37-41 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCADASIL
_xgenetics
650 0 4 _aCohort Studies
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFounder Effect
650 0 4 _aGenotype
650 0 4 _aHaplotypes
650 0 4 _aHumans
650 0 4 _aItaly
650 0 4 _aMutation
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aReceptor, Notch3
650 0 4 _aReceptors, Notch
_xgenetics
650 0 4 _aWhite People
_xgenetics
700 1 _aMalerba, G
700 1 _aFerrarini, M
700 1 _aRagno, M
700 1 _aPradotto, L
700 1 _aMauro, A
700 1 _aFabrizi, G M
773 0 _tJournal of the neurological sciences
_gvol. 319
_gno. 1-2
_gp. 37-41
856 4 0 _uhttps://doi.org/10.1016/j.jns.2012.05.025
_zAvailable from publisher's website
999 _c21835020
_d21835020