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A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.
Rendtorff ND, Zhu M, Fagerheim T, Antal TL, Jones M, Teslovich TM, Gillanders EM, Barmada M, Teig E, Trent JM, Friderici KH, Stephan DA, Tranebjaerg L. Rendtorff ND, et al. Among authors: antal tl. Eur J Hum Genet. 2006 Oct;14(10):1097-105. doi: 10.1038/sj.ejhg.5201670. Epub 2006 Jun 14. Eur J Hum Genet. 2006. PMID: 16773128
Learning spatio-temporal patterns with Neural Cellular Automata.
Richardson AD, Antal T, Blythe RA, Schumacher LJ. Richardson AD, et al. Among authors: antal t. PLoS Comput Biol. 2024 Apr 26;20(4):e1011589. doi: 10.1371/journal.pcbi.1011589. eCollection 2024 Apr. PLoS Comput Biol. 2024. PMID: 38669297 Free PMC article.
Sequential mutations in exponentially growing populations.
Nicholson MD, Cheek D, Antal T. Nicholson MD, et al. Among authors: antal t. PLoS Comput Biol. 2023 Jul 10;19(7):e1011289. doi: 10.1371/journal.pcbi.1011289. eCollection 2023 Jul. PLoS Comput Biol. 2023. PMID: 37428805 Free PMC article.
130 results