(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty.
Suzuki E, Shima H, Kagami M, Soneda S, Tanaka T, Yatsuga S, Nishioka J, Oto Y, Kamiya T, Naiki Y, Ogata T, Fujisawa Y, Nakamura A, Kawashima S, Morikawa S, Horikawa R, Sano S, Fukami M.
Suzuki E, et al. Among authors: yatsuga s.
Hum Genome Var. 2019 Jan 21;6:7. doi: 10.1038/s41439-019-0039-9. eCollection 2019.
Hum Genome Var. 2019.
PMID: 30675365
Free PMC article.