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2. Eren, Erdal, Tezcan Ünlü, Havva, Ceylaner, Serdar, Tarım, Ömer. 2021. Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2. In Journal of clinical research in pediatric endocrinology, 15, 97-102. doi:10.4274/jcrpe.galenos.2021.2020.0315. https://pubmed.ncbi.nlm.nih.gov/34382758/
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4. Müller, Réka, Steffensen, Thora, Krstić, Nevena, Cain, Mary Ashley. 2021. Report of a novel variant in the FAM111A gene in a fetus with multiple anomalies including gracile bones, hypoplastic spleen, and hypomineralized skull. In American journal of medical genetics. Part A, 185, 1903-1907. doi:10.1002/ajmg.a.62182. https://pubmed.ncbi.nlm.nih.gov/33750016/
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6. Yang, Huixia, Kolben, Thomas, Kessler, Mirjana, Jeschke, Udo, von Schönfeldt, Viktoria. 2022. FAM111A Is a Novel Molecular Marker for Oocyte Aging. In Biomedicines, 10, . doi:10.3390/biomedicines10020257. https://pubmed.ncbi.nlm.nih.gov/35203468/
7. Pu, Jian, Xu, Zuoming, Huang, Youguan, Wu, Xianjian, Wei, Huamei. 2023. N6 -methyladenosine-modified FAM111A-DT promotes hepatocellular carcinoma growth via epigenetically activating FAM111A. In Cancer science, 114, 3649-3665. doi:10.1111/cas.15886. https://pubmed.ncbi.nlm.nih.gov/37400994/