1. Shao, Chong, Wang, Yi-Wen, He, Jin-Wei, Wang, Chun, Zhang, Zhen-Lin. 2019. Genetic variants in the PLS3 gene are associated with osteoporotic fractures in postmenopausal Chinese women. In Acta pharmacologica Sinica, 40, 1212-1218. doi:10.1038/s41401-019-0219-7. https://pubmed.ncbi.nlm.nih.gov/30837644/
2. Apperley, Louise J, Albaba, Shadi, Dharmaraj, Poonam, Balasubramanian, Meena. 2022. PLS3 whole gene deletion as a cause of X-linked osteoporosis: Clinical report with review of published PLS3 literature. In Clinical dysmorphology, 32, 43-47. doi:10.1097/MCD.0000000000000442. https://pubmed.ncbi.nlm.nih.gov/36503925/
3. Szkandera, Joanna, Winder, Thomas, Stotz, Michael, Gerger, Armin, Absenger, Gudrun. 2013. A common gene variant in PLS3 predicts colon cancer recurrence in women. In Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 34, 2183-8. doi:10.1007/s13277-013-0754-7. https://pubmed.ncbi.nlm.nih.gov/23549633/
4. Petit, Florence, Longoni, Mauro, Wells, Julie, Donahoe, Patricia K, High, Frances A. 2023. PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects. In American journal of human genetics, 110, 1787-1803. doi:10.1016/j.ajhg.2023.09.002. https://pubmed.ncbi.nlm.nih.gov/37751738/