1. Iturrate, Asier, Rivera-Barahona, Ana, Flores, Carmen-Lisset, Abdalla, Ebtesam, Ruiz-Perez, Victor L. 2022. Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia. In American journal of human genetics, 109, 1828-1849. doi:10.1016/j.ajhg.2022.08.009. https://pubmed.ncbi.nlm.nih.gov/36084634/
2. Howell, Viive M, de Haan, Georgius, Bergren, Sarah, Frankel, Wayne N, Meisler, Miriam H. 2008. A targeted deleterious allele of the splicing factor SCNM1 in the mouse. In Genetics, 180, 1419-27. doi:10.1534/genetics.108.094227. https://pubmed.ncbi.nlm.nih.gov/18791226/
3. Buchner, David A, Trudeau, Michelle, Meisler, Miriam H. . SCNM1, a putative RNA splicing factor that modifies disease severity in mice. In Science (New York, N.Y.), 301, 967-9. doi:. https://pubmed.ncbi.nlm.nih.gov/12920299/
4. Shu, Ze, Wang, Ligang, Wang, Jinbu, Yan, Hua, Wang, Lixian. 2022. Integrative Analysis of Nanopore and Illumina Sequencing Reveals Alternative Splicing Complexity in Pig Longissimus Dorsi Muscle. In Frontiers in genetics, 13, 877646. doi:10.3389/fgene.2022.877646. https://pubmed.ncbi.nlm.nih.gov/35480309/
5. Kasteleijn-Nolst Trenité, Dorothée G A, Volkers, Linda, Strengman, Eric, de Kovel, Carolien G F, Koeleman, Bobby P C. 2015. Clinical and genetic analysis of a family with two rare reflex epilepsies. In Seizure, 29, 90-6. doi:10.1016/j.seizure.2015.03.020. https://pubmed.ncbi.nlm.nih.gov/26076849/
6. Kearney, Jennifer A, Buchner, David A, De Haan, Georgius, Sprunger, Leslie K, Meisler, Miriam H. . Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6). In Human molecular genetics, 11, 2765-75. doi:. https://pubmed.ncbi.nlm.nih.gov/12374766/
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