Neonatal detection of Aicardi Goutières Syndrome by increased C26:0 lysophosphatidylcholine and interferon signature on newborn screening blood spots.

Authors

Thais Armangue
Joseph J Orsini
Asako Takanohashi
Francesco Gavazzi
Alex Conant
Heather Gordish-Dressman, George Washington University
Adeline Vanderver, George Washington University
+several additional authors

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