1. Paine, Ingrid, Posey, Jennifer E, Grochowski, Christopher M, Lyon, Gholson J, Lupski, James R. 2019. Paralog Studies Augment Gene Discovery: DDX and DHX Genes. In American journal of human genetics, 105, 302-316. doi:10.1016/j.ajhg.2019.06.001. https://pubmed.ncbi.nlm.nih.gov/31256877/
2. Hautakangas, Milla-Riikka, Widgren, Paula, Korpelainen, Paavo, Hinttala, Reetta, Uusimaa, Johanna. 2023. Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variant. In Clinical genetics, 104, 686-693. doi:10.1111/cge.14416. https://pubmed.ncbi.nlm.nih.gov/37574199/
3. Putiri, Emily, Pelegri, Francisco. 2011. The zebrafish maternal-effect gene mission impossible encodes the DEAH-box helicase Dhx16 and is essential for the expression of downstream endodermal genes. In Developmental biology, 353, 275-89. doi:10.1016/j.ydbio.2011.03.001. https://pubmed.ncbi.nlm.nih.gov/21396359/
4. Gencheva, Marieta, Lin, Ting-Yu, Wu, Xiwei, Lin, Shwu-Bin, Lin, Ren-Jang. 2010. Nuclear retention of unspliced pre-mRNAs by mutant DHX16/hPRP2, a spliceosomal DEAH-box protein. In The Journal of biological chemistry, 285, 35624-32. doi:10.1074/jbc.M110.122309. https://pubmed.ncbi.nlm.nih.gov/20841358/
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