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Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

Year: 2013
Type: article
DOI: 10.1038/nature11922">https://dx.doi.org/10.1038/nature11922</a
Authors: Kim, Hong Joo, Kim, Nam Chul, Wang, Yong-Dong, Scarborough, Emily A., Moore, Jennifer, Diaz, Zamia, MacLea, Kyle S., Freibaum, Brain, Li, Songqing, Molliex, Amandine, Kanagaraj, Anderson P., Carter, Robert, Boylan, Kevin B., Wojtas, Aleksandra M., Rademakers, Rosa, Pinkus, Jack L., Greenberg, Steven A., Trojanowski, John Q., Traynor, Bryan J., Smith, Bradley N.
Institutions: St. Jude Children's Research Hospital, University of Pennsylvania, Colorado State University, Mayo Clinic, Mayo Clinic in Florida, Brigham and Women's Hospital, Harvard University, National Institutes of Health, National Institute on Aging
Language: English
Subfield: Neurology
Field: Medicine
Open Access status: closed
OpenAlex ID: W7134239755
FWCI:
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