Identification of rare missense mutations in...

Gynecological Endocrinology 2020 / 05

Identification of rare missense mutations in NOTCH2 and HERC2 associated with familial central precocious puberty via whole-exome sequencing

Lee, Hae Sang, Jeong, Hwal Rim, Rho, Jung Gi, Kum, Chang Dae, Kim, Kyung Hee, Kim, Do Wan, Cheong, Jae Youn, Jeong, Seon-Yong, Hwang, Jin Soon
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Journal:
Gynecological Endocrinology
DOI:
10.1080/09513590.2020.1760241
Date:
May, 2020
File:
PDF, 970 KB
2020
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