1. Sener, Elif Funda, Onal, Muge Gulcihan, Dal, Fatma, Canatan, Halit, Oztop, Didem Behice. 2020. Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorder. In The International journal of neuroscience, 132, 1072-1079. doi:10.1080/00207454.2020.1860968. https://pubmed.ncbi.nlm.nih.gov/33287601/
2. Sener, Elif Funda, Cıkılı Uytun, Merve, Korkmaz Bayramov, Keziban, Canatan, Halit, Ozkul, Yusuf. 2016. The roles of CC2D1A and HTR1A gene expressions in autism spectrum disorders. In Metabolic brain disease, 31, 613-9. doi:10.1007/s11011-016-9795-0. https://pubmed.ncbi.nlm.nih.gov/26782176/
3. Bhattacharya, Aniket, Parlanti, Paola, Cavallo, Luca, Mari, Francesca, Manzini, M Chiara. . A novel framework for functional annotation of variants of uncertain significance in ID/ASD risk gene CC2D1A. In Human molecular genetics, 33, 1229-1240. doi:10.1093/hmg/ddae070. https://pubmed.ncbi.nlm.nih.gov/38652285/
4. Rogaeva, Anastasia, Galaraga, Kimberly, Albert, Paul R. . The Freud-1/CC2D1A family: transcriptional regulators implicated in mental retardation. In Journal of neuroscience research, 85, 2833-8. doi:. https://pubmed.ncbi.nlm.nih.gov/17394259/
5. Basel-Vanagaite, L, Attia, R, Yahav, M, Simon, A J, Shohat, M. 2005. The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation. In Journal of medical genetics, 43, 203-10. doi:. https://pubmed.ncbi.nlm.nih.gov/16033914/
6. Shi, Zhang-Yan, Li, Ya-Jing, Zhang, Ke-Jin, Han, Ning, Zhang, Fu-Chang. 2011. Positive association of CC2D1A and CC2D2A gene haplotypes with mental retardation in a Han Chinese population. In DNA and cell biology, 31, 80-7. doi:10.1089/dna.2011.1253. https://pubmed.ncbi.nlm.nih.gov/22023432/
7. Rashvand, Zahra, Najmabadi, Hossein, Kahrizi, Kimia, Najafipour, Reza, Omrani, Mir Davood. 2024. Identification of a Novel Variant in CC2D1A Gene Linked to Autosomal Recessive Intellectual Disability 3 in an Iranian Family and Investigating the Structure and Pleiotropic Effects of this Gene. In Iranian journal of child neurology, 18, 25-41. doi:10.22037/ijcn.v18i1.42188. https://pubmed.ncbi.nlm.nih.gov/38375126/
8. Kim, Angelina Haesoo, Sakin, Irmak, Viviano, Stephen, Temel, Sehime G, Deniz, Engin. 2024. CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. In Life science alliance, 7, . doi:10.26508/lsa.202402708. https://pubmed.ncbi.nlm.nih.gov/39168639/
9. Yang, Cheng-Yi, Hung, Yu-Chieh, Cheng, Kuan-Hsiang, Ling, Pin, Hsu, Kuei-Sen. 2021. Loss of CC2D1A in Glutamatergic Neurons Results in Autistic-Like Features in Mice. In Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 18, 2021-2039. doi:10.1007/s13311-021-01072-z. https://pubmed.ncbi.nlm.nih.gov/34132974/
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