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Xina B 1
Showing records 1 to 1 | Display all abstracts from Xina B45518 Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke
Xina B; Jonesb S; Puffenbergerc EG; Hinzee C; Brighta A; Tanf H; Zhouf A; Wub G; Vargus-Adamse J; Agamanolisg D
Proceedings of the National Academy of Sciences of the United States of America 2011; 108: 5372-5377
