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IFT172 as the 19th gene causative of oral-facial-digital syndrome.
Yamada M, Uehara T, Suzuki H, Takenouchi T, Fukushima H, Morisada N, Tominaga K, Onoda M, Kosaki K. Yamada M, et al. Among authors: morisada n. Am J Med Genet A. 2019 Dec;179(12):2510-2513. doi: 10.1002/ajmg.a.61373. Epub 2019 Oct 6. Am J Med Genet A. 2019. PMID: 31587445 No abstract available.
Clinical spectrum of male patients with OFD1 mutations.
Sakakibara N, Morisada N, Nozu K, Nagatani K, Ohta T, Shimizu J, Wada T, Shima Y, Yamamura T, Minamikawa S, Fujimura J, Horinouchi T, Nagano C, Shono A, Ye MJ, Nozu Y, Nakanishi K, Iijima K. Sakakibara N, et al. Among authors: morisada n. J Hum Genet. 2019 Jan;64(1):3-9. doi: 10.1038/s10038-018-0532-x. Epub 2018 Nov 6. J Hum Genet. 2019. PMID: 30401917
De novo NSF mutations cause early infantile epileptic encephalopathy.
Suzuki H, Yoshida T, Morisada N, Uehara T, Kosaki K, Sato K, Matsubara K, Takano-Shimizu T, Takenouchi T. Suzuki H, et al. Among authors: morisada n. Ann Clin Transl Neurol. 2019 Nov;6(11):2334-2339. doi: 10.1002/acn3.50917. Epub 2019 Nov 1. Ann Clin Transl Neurol. 2019. PMID: 31675180 Free PMC article.
A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy.
Shishido A, Morisada N, Tominaga K, Uemura H, Haruna A, Hanafusa H, Nozu K, Iijima K. Shishido A, et al. Among authors: morisada n. Hum Genome Var. 2020 Aug 17;7:23. doi: 10.1038/s41439-020-00110-0. eCollection 2020. Hum Genome Var. 2020. PMID: 32864149 Free PMC article.
Genome Analysis in Sick Neonates and Infants: High-yield Phenotypes and Contribution of Small Copy Number Variations.
Suzuki H, Nozaki M, Yoshihashi H, Imagawa K, Kajikawa D, Yamada M, Yamaguchi Y, Morisada N, Eguchi M, Ohashi S, Ninomiya S, Seto T, Tokutomi T, Hida M, Toyoshima K, Kondo M, Inui A, Kurosawa K, Kosaki R, Ito Y, Okamoto N, Kosaki K, Takenouchi T. Suzuki H, et al. Among authors: morisada n. J Pediatr. 2022 May;244:38-48.e1. doi: 10.1016/j.jpeds.2022.01.033. Epub 2022 Feb 4. J Pediatr. 2022. PMID: 35131284 Free article.
Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics.
Matsunoshita N, Nozu K, Shono A, Nozu Y, Fu XJ, Morisada N, Kamiyoshi N, Ohtsubo H, Ninchoji T, Minamikawa S, Yamamura T, Nakanishi K, Yoshikawa N, Shima Y, Kaito H, Iijima K. Matsunoshita N, et al. Among authors: morisada n. Genet Med. 2016 Feb;18(2):180-8. doi: 10.1038/gim.2015.56. Epub 2015 Apr 16. Genet Med. 2016. PMID: 25880437 Free article.
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