1. Paul, Maimuna S, Michener, Sydney L, Pan, Hongling, Lee, Brendan H, Chao, Hsiao-Tuan. . A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3. In American journal of human genetics, 111, 96-118. doi:10.1016/j.ajhg.2023.12.004. https://pubmed.ncbi.nlm.nih.gov/38181735/
2. Fu, Fangmei, Niu, Rui, Zheng, Minying, Fu, Wenzheng, Zhang, Shiwu. 2023. Clinicopathological Significances and Prognostic Value of PPFIA4 in Colorectal Cancer. In Journal of Cancer, 14, 24-34. doi:10.7150/jca.78634. https://pubmed.ncbi.nlm.nih.gov/36605492/
3. Paul, Maimuna S, Michener, Sydney L, Pan, Hongling, Lee, Brendan H, Chao, Hsiao-Tuan. 2023. Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy. In medRxiv : the preprint server for health sciences, , . doi:10.1101/2023.03.27.23287689. https://pubmed.ncbi.nlm.nih.gov/37034625/
4. Specchio, Nicola, Di Micco, Valentina, Aronica, Eleonora, Trivisano, Marina, Curatolo, Paolo. 2025. The epilepsy-autism phenotype associated with developmental and epileptic encephalopathies: New mechanism-based therapeutic options. In Epilepsia, , . doi:10.1111/epi.18209. https://pubmed.ncbi.nlm.nih.gov/39985505/
5. Li, Wen-han, Zhou, Zhang-jian, Huang, Tian-he, Song, Yong-chun, Chang, Dong-min. 2016. Detection of OSR2, VAV3, and PPFIA3 Methylation in the Serum of Patients with Gastric Cancer. In Disease markers, 2016, 5780538. doi:10.1155/2016/5780538. https://pubmed.ncbi.nlm.nih.gov/27143812/
6. Viswanathan, Sindhu, Oliver, Karen L, Regan, Brigid M, Mefford, Heather C, Scheffer, Ingrid E. 2024. Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS). In Annals of neurology, 96, 932-943. doi:10.1002/ana.27041. https://pubmed.ncbi.nlm.nih.gov/39096015/
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