1. Alhaidari, Abdulmajeed I, Albakri, Amani S, Alhumaidi, Suzan S. 2022. A Novel PGAP3 Gene Mutation-Related Megalocornea Can Be Misdiagnosed as Primary Congenital Glaucoma. In Cureus, 14, e29387. doi:10.7759/cureus.29387. https://pubmed.ncbi.nlm.nih.gov/36304370/
2. Maddirevula, Sateesh, Alsahli, Saud, Alhabeeb, Lamees, Shaheen, Ranad, Alkuraya, Fowzan S. 2018. Expanding the phenome and variome of skeletal dysplasia. In Genetics in medicine : official journal of the American College of Medical Genetics, 20, 1609-1616. doi:10.1038/gim.2018.50. https://pubmed.ncbi.nlm.nih.gov/29620724/
3. Heft Neal, Molly E, Birkeland, Andrew C, Bhangale, Apurva D, McKean, Erin L, Brenner, J Chad. 2021. Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene. In BMC cancer, 21, 636. doi:10.1186/s12885-021-08370-x. https://pubmed.ncbi.nlm.nih.gov/34051734/
4. Wang, Dong, Hao, Siyu, He, Hongjie, Fu, Songbin, Yu, Jingcui. 2023. Contribution of PGAP3 co-amplified and co-overexpressed with ERBB2 at 17q12 involved poor prognosis in gastric cancer. In Journal of cellular and molecular medicine, 27, 2424-2436. doi:10.1111/jcmm.17828. https://pubmed.ncbi.nlm.nih.gov/37386793/
5. Thompson, Miles D, Li, Xueying, Spencer-Manzon, Michele, Kinoshita, Taroh, Carpenter, Thomas O. 2023. Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3). In Genes, 14, . doi:10.3390/genes14020359. https://pubmed.ncbi.nlm.nih.gov/36833286/
6. Sakaguchi, Tomohiro, Žigman, Tamara, Petković Ramadža, Danijela, Matsumoto, Naomichi, Barić, Ivo. 2018. A novel PGAP3 mutation in a Croatian boy with brachytelephalangy and a thin corpus callosum. In Human genome variation, 5, 18005. doi:10.1038/hgv.2018.5. https://pubmed.ncbi.nlm.nih.gov/29531774/
7. Abdel-Hamid, M S, Issa, M Y, Otaify, G A, Elbendary, H M, Zaki, M S. 2017. PGAP3-related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation. In Clinical genetics, 93, 84-91. doi:10.1111/cge.13033. https://pubmed.ncbi.nlm.nih.gov/28390064/
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