1. Cui, Sheng, Shin, Yoo Jin, Fang, Xianying, Yang, Chul Woo, Chung, Byung Ha. 2023. CRISPR/Cas9-mediated A4GALT suppression rescues Fabry disease phenotypes in a kidney organoid model. In Translational research : the journal of laboratory and clinical medicine, 258, 35-46. doi:10.1016/j.trsl.2023.02.005. https://pubmed.ncbi.nlm.nih.gov/36805562/
2. Chen, Qing, Xiao, Jianyu, Duan, Zhimin, Huang, Chengyin, Li, Min. 2020. Novel A4GALT gene variation with rare p phenotype in a compound heterozygous Chinese individual. In Transfusion, 61, E5-E6. doi:10.1111/trf.16163. https://pubmed.ncbi.nlm.nih.gov/33111355/
3. Shastry, Shamee, Satyamoorthy, Kapaettu, Acharya, Kiran V, Reghunathan, Dinesh, Joshi, Manjunath B. 2019. Deletion in the A4GALT Gene Associated with Rare "P null" Phenotype: The First Report from India. In Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie, 47, 186-189. doi:10.1159/000501916. https://pubmed.ncbi.nlm.nih.gov/32355479/
4. Lai, Yin-Ju, Wu, Wan-Yi, Yang, Chen-Ming, Lin, Marie, Yu, Lung-Chih. 2014. A systematic study of single-nucleotide polymorphisms in the A4GALT gene suggests a molecular genetic basis for the P1/P2 blood groups. In Transfusion, 54, 3222-31. doi:10.1111/trf.12771. https://pubmed.ncbi.nlm.nih.gov/25041587/
5. Hellberg, Asa, Schmidt-Melbye, Anne-Christine, Reid, Marion E, Olsson, Martin L. 2007. Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype. In Transfusion, 48, 479-87. doi:. https://pubmed.ncbi.nlm.nih.gov/18067504/
6. Yeh, Chih-Chun, Chang, Ching-Jin, Twu, Yuh-Ching, Lin, Sheng-Wei, Yu, Lung-Chih. 2018. The differential expression of the blood group P1 -A4GALT and P2 -A4GALT alleles is stimulated by the transcription factor early growth response 1. In Transfusion, 58, 1054-1064. doi:10.1111/trf.14515. https://pubmed.ncbi.nlm.nih.gov/29399809/
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