Heterozygous rare genetic variants in non-syndromic early-onset obesity
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Medicine (miscellaneous)
Link
http://www.nature.com/articles/s41366-019-0357-5.pdf
Reference65 articles.
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4. Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, Komoto Y, et al. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome. Nat Genet. 1996;14:171–3.
5. Martos-Moreno GÁ, Serra-Juhé C, Pérez-Jurado LA, Argente J. Underdiagnosed Beckwith–Wiedemann syndrome among early onset obese children. Arch Dis Child. 2014;99:965–7.
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