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CACNA1S mutation-associated dental anomalies: A calcium channelopathy.
Kantaputra P, Butali A, Eliason S, Chalkley C, Nakornchai S, Bongkochwilawan C, Kawasaki K, Kumchiang A, Ngamphiw C, Tongsima S, Ketudat Cairns JR, Olsen B, Intachai W, Ohazama A, Tucker AS, Amendt BA. Kantaputra P, et al. Among authors: bongkochwilawan c. Oral Dis. 2024 Apr;30(3):1350-1359. doi: 10.1111/odi.14551. Epub 2023 Mar 13. Oral Dis. 2024. PMID: 36825457
Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation.
Kantaputra PN, Bongkochwilawan C, Kaewgahya M, Ohazama A, Kayserili H, Erdem AP, Aktoren O, Guven Y. Kantaputra PN, et al. Among authors: bongkochwilawan c. Am J Med Genet A. 2014 Aug;164A(8):2124-8. doi: 10.1002/ajmg.a.36579. Epub 2014 Apr 22. Am J Med Genet A. 2014. PMID: 24756937 No abstract available.
Periodontal disease and FAM20A mutations.
Kantaputra PN, Bongkochwilawan C, Lubinsky M, Pata S, Kaewgahya M, Tong HJ, Ketudat Cairns JR, Guven Y, Chaisrisookumporn N. Kantaputra PN, et al. Among authors: bongkochwilawan c. J Hum Genet. 2017 Jul;62(7):679-686. doi: 10.1038/jhg.2017.26. Epub 2017 Mar 16. J Hum Genet. 2017. PMID: 28298625