A mutation in the nuclear speckle and splicing factor SRRM2 is associated with multisystem proteinopathy and causes dysregulation of synapse-associated genes
| Authors | Qingyu Shi, Chloe Lauder, Jolie Marie Miller, Yong-Dong Wang, Noha Elsakrmy, Sofija Volkanoska, Brian D Freibaum, Joanne Wu, Michael Benatar, Hui Peng, Hong Joo Kim, J Paul Taylor, Haissi Cui |
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| DOI | 10.1261/rna.080836.125 |
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| Source | View on PubMed |
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