000 01172 a2200385 4500
005 20250518090454.0
264 0 _c20200723
008 202007s 0 0 eng d
022 _a1471-2377
024 7 _a10.1186/s12883-020-01660-0
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHe, Ruojie
245 0 0 _aHomozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report.
_h[electronic resource]
260 _bBMC neurology
_cMar 2020
300 _a72 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAsian People
_xgenetics
650 0 4 _aBrain
_xpathology
650 0 4 _aCADASIL
_xgenetics
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aReceptor, Notch3
_xgenetics
700 1 _aLi, Huan
700 1 _aSun, Yiming
700 1 _aChen, Menglong
700 1 _aWang, Liang
700 1 _aZhu, Yuling
700 1 _aZhang, Cheng
773 0 _tBMC neurology
_gvol. 20
_gno. 1
_gp. 72
856 4 0 _uhttps://doi.org/10.1186/s12883-020-01660-0
_zAvailable from publisher's website
999 _c30696022
_d30696022