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2. Alasmari, Badriah G, Elzubair, Khalid, Alquraishi, Ali, Elzubair, Lina, Al Tala, Saeed. 2024. A Rare THPO Gene Mutation in a Saudi Female Child: A Case Report and Literature Review. In Cureus, 16, e70513. doi:10.7759/cureus.70513. https://pubmed.ncbi.nlm.nih.gov/39479124/
3. Capaci, Valeria, Adam, Etai, Bar-Joseph, Ifat, Pecci, Alessandro, Savoia, Anna. 2023. Defective binding of ETS1 and STAT4 due to a mutation in the promoter region of THPO as a novel mechanism of congenital amegakaryocytic thrombocytopenia. In Haematologica, 108, 1385-1393. doi:10.3324/haematol.2022.281392. https://pubmed.ncbi.nlm.nih.gov/36226497/
4. Kimura, Hiroyuki, Onozawa, Masahiro, Matsukawa, Toshihiro, Kondo, Takeshi, Teshima, Takanori. 2024. Relative impact of THPO mutation causing hereditary thrombocythemia. In Experimental hematology, 134, 104208. doi:10.1016/j.exphem.2024.104208. https://pubmed.ncbi.nlm.nih.gov/38548144/
5. Kimura, Hiroyuki, Onozawa, Masahiro, Hashiguchi, Junichi, Matsuno, Yoshihiro, Teshima, Takanori. 2023. Hereditary thrombocythemia due to splicing donor site mutation of THPO in a Japanese family. In Annals of hematology, 103, 89-96. doi:10.1007/s00277-023-05523-9. https://pubmed.ncbi.nlm.nih.gov/37962621/
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