Neonatal detection of Aicardi Goutières Syndrome by increased C26:0 lysophosphatidylcholine and interferon signature on newborn screening blood spots.
Document Type
Journal Article
Publication Date
7-20-2017
Journal
Molecular Genetics and Metabolism
DOI
10.1016/j.ymgme.2017.07.006
APA Citation
Armangue, T., Orsini, J., Takanohashi, A., Gavazzi, F., Conant, A., Gordish-Dressman, H., Vanderver, A., & +several additional authors (2017). Neonatal detection of Aicardi Goutières Syndrome by increased C26:0 lysophosphatidylcholine and interferon signature on newborn screening blood spots.. Molecular Genetics and Metabolism, (). http://dx.doi.org/10.1016/j.ymgme.2017.07.006
Peer Reviewed
1
