1. Kaufman, Carolyn S, Butler, Merlin G. . Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome. In World journal of medical genetics, 6, 17-21. doi:10.5496/wjmg.v6.i2.17. https://pubmed.ncbi.nlm.nih.gov/28344932/
2. Liang, Guozheng, Wang, ShengPeng, Shao, Jingchen, Wang, Lei, Offermanns, Stefan. 2022. Tenascin-X Mediates Flow-Induced Suppression of EndMT and Atherosclerosis. In Circulation research, 130, 1647-1659. doi:10.1161/CIRCRESAHA.121.320694. https://pubmed.ncbi.nlm.nih.gov/35443807/
3. Gao, Yinjie, Lu, Lin, Yu, Bingqing, Nie, Min, Wu, Xueyan. . The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency. In The Journal of clinical endocrinology and metabolism, 105, . doi:10.1210/clinem/dgaa199. https://pubmed.ncbi.nlm.nih.gov/32291442/
4. Mirza, Nida, Upadhyaya, Sundeep, Mehta, Sagar, Malhotra, Smita, Sibal, Anupam. 2021. Esophageal Stricture and Dermal Pathology Related to Compound Heterozygous Mutations in the TNXB Gene. In Journal of pediatric genetics, 12, 224-226. doi:10.1055/s-0041-1724048. https://pubmed.ncbi.nlm.nih.gov/37575646/
5. Marino, Roxana, Moresco, Angélica, Perez Garrido, Natalia, Ramirez, Pablo, Belgorosky, Alicia. 2022. Congenital Adrenal Hyperplasia and Ehlers-Danlos Syndrome. In Frontiers in endocrinology, 13, 803226. doi:10.3389/fendo.2022.803226. https://pubmed.ncbi.nlm.nih.gov/35282436/
6. Marino, Roxana, Garrido, Natalia Perez, Ramirez, Pablo, Soria, Ianina, Belgorosky, Alicia. . Ehlers-Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia. In The Journal of clinical endocrinology and metabolism, 106, e2789-e2802. doi:10.1210/clinem/dgab033. https://pubmed.ncbi.nlm.nih.gov/33482002/