Identification of rare missense mutations in NOTCH2 and HERC2 associated with familial central precocious puberty via whole-exome sequencing-Reference-Cited by-同舟云学术

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

Author:

Lee Hae Sang¹^ORCID,Jeong Hwal Rim²,Rho Jung Gi¹,Kum Chang Dae¹,Kim Kyung Hee¹,Kim Do Wan³,Cheong Jae Youn³⁴,Jeong Seon-Yong⁵⁶,Hwang Jin Soon¹

Affiliation:

1. Department of Pediatrics, Ajou University School of Medicine, Suwon, Republic of Korea;

2. Department of Pediatrics, Soonchunhyang University Cheonan Hospital, Soonchunhyang University College of Medicine, Cheonan, Korea;

3. Ajou Translational Omics Center, Ajou University Medical Center, Suwon, Republic of Korea;

4. Department of Gastroenterology, Ajou University School of Medicine, Suwon, Republic of Korea;

5. Department of Medical Genetics, Ajou University School of Medicine, Suwon, Republic of Korea;

6. Department of Biomedical Sciences, Ajou University Graduate School of Medicine, Suwon, Republic of Korea

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

Reference34 articles.

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