TY  - GEN
AU  - Xin,Baozhong
AU  - Jones,Stephen
AU  - Puffenberger,Erik G
AU  - Hinze,Claas
AU  - Bright,Alicia
AU  - Tan,Haiyan
AU  - Zhou,Aimin
AU  - Wu,Guiyun
AU  - Vargus-Adams,Jilda
AU  - Agamanolis,Dimitris
AU  - Wang,Heng
TI  - Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke
SN  - 1091-6490
PY  - 2011///0610
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Base Sequence
KW  - Cerebrovascular Circulation
KW  - Cerebrovascular Disorders
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - DNA Mutational Analysis
KW  - Ethnicity
KW  - Female
KW  - Homozygote
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Monomeric GTP-Binding Proteins
KW  - Mutation
KW  - Pedigree
KW  - SAM Domain and HD Domain-Containing Protein 1
KW  - Stroke
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1073/pnas.1014265108
ER  -