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The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.
Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N. Yamada Y, et al. Among authors: kajita m. Am J Med Genet A. 2014 Aug;164A(8):1899-908. doi: 10.1002/ajmg.a.36551. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715670
Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1.
Tanizawa Y, Matsuda K, Matsuo M, Ohta Y, Ochi N, Adachi M, Koga M, Mizuno S, Kajita M, Tanaka Y, Tachibana K, Inoue H, Furukawa S, Amachi T, Ueda K, Oka Y. Tanizawa Y, et al. Among authors: kajita m. Diabetes. 2000 Jan;49(1):114-20. doi: 10.2337/diabetes.49.1.114. Diabetes. 2000. PMID: 10615958
A case of infantile febrile psoriasiform dermatitis.
Tsuge I, Fujii H, Andou Y, Katayama I, Kajita M, Haga Y, Asano K, Mori O, Matsumoto Y, Ohashi M, et al. Tsuge I, et al. Among authors: kajita m. Pediatr Dermatol. 1995 Mar;12(1):28-34. doi: 10.1111/j.1525-1470.1995.tb00120.x. Pediatr Dermatol. 1995. PMID: 7792216
230 results