Structural genomic variation in ischemic stroke

Technological advances in molecular genetics allow rapid and sensitive identification of genomic copy number variants (CNVs). This, in turn, has sparked interest in the function such variation may play in disease. While a role for copy number mutations as a cause of Mendelian disorders is well estab...

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Detalhes bibliográficos
Main Authors: Matarin, Mar, Simon-Sanchez, Javier, Fung, Hon-Chung, Scholz, Sonja, Gibbs, J. Raphael, Hernandez, Dena G., Crews, Cynthia, Britton, Angela, Wavrant De Vrieze, Fabienne, Brott, Thomas G., Brown, Robert D., Worrall, Bradford B., Silliman, Scott, Case, L. Douglas, Hardy, John A., Rich, Stephen S., Meschia, James F., Singleton, Andrew B.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2730937/
https://ncbi.nlm.nih.gov/pubmed/18288507
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-008-0119-3
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