1. Othman, Maha, Emsley, Jonas. 2017. Gene of the issue: GP1BA gene mutations associated with bleeding. In Platelets, 28, 832-836. doi:10.1080/09537104.2017.1361526. https://pubmed.ncbi.nlm.nih.gov/28961024/
2. Zhang, Senlin, Ling, Jing, Cui, Kai, Fan, Junjie, Hu, Shaoyan. 2024. Bernard-Soulier syndrome caused by two novel heterozygous GP1BA gene mutations: a case report and literature review. In Hematology (Amsterdam, Netherlands), 29, 2334642. doi:10.1080/16078454.2024.2334642. https://pubmed.ncbi.nlm.nih.gov/38564005/
3. Ma, Jingyao, Chen, Zhenping, Li, Gang, Gu, Hao, Wu, Runhui. 2021. A novel mutation in GP1BA gene in a family with autosomal dominant Bernard Soulier syndrome variant: A case report. In Experimental and therapeutic medicine, 21, 360. doi:10.3892/etm.2021.9791. https://pubmed.ncbi.nlm.nih.gov/33732333/
4. Mishra, Aniket, Malik, Rainer, Hachiya, Tsuyoshi, Dichgans, Martin, Debette, Stephanie. 2022. Stroke genetics informs drug discovery and risk prediction across ancestries. In Nature, 611, 115-123. doi:10.1038/s41586-022-05165-3. https://pubmed.ncbi.nlm.nih.gov/36180795/
5. Özdemir, Zeynep C, Düzenli Kar, Yeter, Ceylaner, Serdar, Bör, Özcan. . A novel mutation in the GP1BA gene in Bernard-Soulier syndrome. In Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 31, 83-86. doi:10.1097/MBC.0000000000000868. https://pubmed.ncbi.nlm.nih.gov/31789661/
6. Martinez-Navajas, Gonzalo, Ceron-Hernandez, Jorge, Simon, Iris, Tersteeg, Claudia, Real, Pedro J. 2023. Lentiviral gene therapy reverts GPIX expression and phenotype in Bernard-Soulier syndrome type C. In Molecular therapy. Nucleic acids, 33, 75-92. doi:10.1016/j.omtn.2023.06.008. https://pubmed.ncbi.nlm.nih.gov/37416759/
7. Dogra, Rupinder Kaur, Das, Reena, Ahluwalia, Jasmina, Kumar, Rohit Manoj, Talwar, K K. . Prothrombotic gene polymorphisms and plasma factors in young North Indian survivors of acute myocardial infarction. In Journal of thrombosis and thrombolysis, 34, 276-82. doi:10.1007/s11239-012-0734-6. https://pubmed.ncbi.nlm.nih.gov/22535530/
8. Ali, Shahnaz, Shetty, Shrimati, Ghosh, Kanjaksha. . A novel mutation in GP1BA gene leads to mono-allelic Bernard Soulier syndrome form of macrothrombocytopenia. In Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 28, 94-95. doi:10.1097/MBC.0000000000000530. https://pubmed.ncbi.nlm.nih.gov/26849716/
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