000 01201 a2200349 4500
005 20250513131912.0
264 0 _c19971224
008 199712s 0 0 eng d
022 _a0140-6736
024 7 _a10.1016/S0140-6736(97)22047-7
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGoate, A M
245 0 0 _aNotch3 mutations and the potential for diagnostic testing for CADASIL.
_h[electronic resource]
260 _bLancet (London, England)
_cNov 1997
300 _a1490 p.
_bdigital
500 _aPublication Type: Journal Article; Comment
650 0 4 _aAdult
650 0 4 _aCerebral Arterial Diseases
_xdiagnosis
650 0 4 _aCerebral Infarction
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aLeukoencephalopathy, Progressive Multifocal
_xdiagnosis
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aProto-Oncogene Proteins
_xgenetics
650 0 4 _aReceptor, Notch3
650 0 4 _aReceptors, Cell Surface
650 0 4 _aReceptors, Notch
700 1 _aMorris, J C
773 0 _tLancet (London, England)
_gvol. 350
_gno. 9090
_gp. 1490
856 4 0 _uhttps://doi.org/10.1016/S0140-6736(97)22047-7
_zAvailable from publisher's website
999 _c9358180
_d9358180