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Science (New York, N.Y.)|February 16, 2019
Heterochromatin anomalies and double-stranded RNA accumulation underlie <i>C9orf72</i> poly(PR) toxicityYong-Jie Zhang, Lin Guo, Patrick K Gonzales, et al.Nature|February 24, 2022
TDP-43 represses cryptic exon inclusion in the FTD-ALS gene UNC13AX Rosa Ma, Mercedes Prudencio, Yuka Koike, et al.Nature|March 5, 2013
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALSHong Joo Kim, Nam Chul Kim, Yong-Dong Wang, et al.Proceedings of the National Academy of Sciences of the United States of America|November 9, 2011
A yeast functional screen predicts new candidate ALS disease genesJulien Couthouis, Michael P Hart, James Shorter, et al.Nature Communications|April 28, 2022
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophyHong Joo Kim, Payam Mohassel, Sandra Donkervoort, et al.Pageof 19