000 01662 a2200517 4500
005 20250517183405.0
264 0 _c20190711
008 201907s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/WNL.0000000000004710
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPreethish-Kumar, Veeramani
245 0 0 _aCARASIL families from India with 3 novel null mutations in the
_h[electronic resource]
260 _bNeurology
_c12 2017
300 _a2392-2394 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aAlopecia
_xdiagnostic imaging
650 0 4 _aCerebral Infarction
_xdiagnostic imaging
650 0 4 _aFemale
650 0 4 _aHigh-Temperature Requirement A Serine Peptidase 1
_xgenetics
650 0 4 _aHumans
650 0 4 _aIndia
650 0 4 _aLeukoencephalopathies
_xdiagnostic imaging
650 0 4 _aLoss of Function Mutation
_xgenetics
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aSpinal Diseases
_xdiagnostic imaging
650 0 4 _aYoung Adult
700 1 _aNozaki, Hiroaki
700 1 _aTiwari, Sarbesh
700 1 _aVengalil, Seena
700 1 _aBhat, Maya
700 1 _aPrasad, Chandrajit
700 1 _aOnodera, Osamu
700 1 _aUemura, Masahiro
700 1 _aDoniparthi, Seshagiri
700 1 _aSaini, Jitender
700 1 _aNashi, Saraswati
700 1 _aPolavarapu, Kiran
700 1 _aNalini, Atchayaram
773 0 _tNeurology
_gvol. 89
_gno. 23
_gp. 2392-2394
856 4 0 _uhttps://doi.org/10.1212/WNL.0000000000004710
_zAvailable from publisher's website
999 _c27752372
_d27752372