Ann Pediatr Endocrinol Metab.  2023 Dec;28(Suppl 1):S20-S22. 10.6065/apem.2244070.035.

A novel compound variant in GNRHR causing congenital idiopathic hypogonadotropic hypogonadism in a young male Korean patient

• Lee G
• Lee MS
• Lee R
• Moon JE

• KMID: 2549334
• DOI: http://doi.org/10.6065/apem.2244070.035

Figure

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  Fig. 1. Sanger sequencing results for GNRHR variants in the patient. Electropherograms of the 2 variants ([A] c.113G>A and [B] c.514G>A) are presented.

Reference

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