000 01893 a2200577 4500
005 20250516030302.0
264 0 _c20110610
008 201106s 0 0 eng d
022 _a1091-6490
024 7 _a10.1073/pnas.1014265108
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aXin, Baozhong
245 0 0 _aHomozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke.
_h[electronic resource]
260 _bProceedings of the National Academy of Sciences of the United States of America
_cMar 2011
300 _a5372-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAge of Onset
650 0 4 _aBase Sequence
650 0 4 _aCerebrovascular Circulation
650 0 4 _aCerebrovascular Disorders
_xgenetics
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDNA Mutational Analysis
650 0 4 _aEthnicity
_xgenetics
650 0 4 _aFemale
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aMonomeric GTP-Binding Proteins
_xgenetics
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aSAM Domain and HD Domain-Containing Protein 1
650 0 4 _aStroke
_xgenetics
650 0 4 _aYoung Adult
700 1 _aJones, Stephen
700 1 _aPuffenberger, Erik G
700 1 _aHinze, Claas
700 1 _aBright, Alicia
700 1 _aTan, Haiyan
700 1 _aZhou, Aimin
700 1 _aWu, Guiyun
700 1 _aVargus-Adams, Jilda
700 1 _aAgamanolis, Dimitris
700 1 _aWang, Heng
773 0 _tProceedings of the National Academy of Sciences of the United States of America
_gvol. 108
_gno. 13
_gp. 5372-7
856 4 0 _uhttps://doi.org/10.1073/pnas.1014265108
_zAvailable from publisher's website
999 _c20674183
_d20674183