Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke-Reference-Cited by-同舟云学术

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Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke

Published:2011-03-14 Issue:13 Volume:108 Page:5372-5377
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Xin B.,Jones S.,Puffenberger E. G.,Hinze C.,Bright A.,Tan H.,Zhou A.,Wu G.,Vargus-Adams J.,Agamanolis D.,Wang H.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference24 articles.

1. Cerebrovascular disease and stroke

2. Pediatric stroke: current developments

3. The role of genetics in stroke

4. SAM as a protein interaction domain involved in developmental regulation

5. SAM domains: uniform structure, diversity of function

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