Cite
First female Korean child with Coffin-Lowry syndrome: a novel variant in RPS6KA3 diagnosed by exome sequencing and a literature review.
MLA
Ari Song, et al. “First Female Korean Child with Coffin-Lowry Syndrome: A Novel Variant in RPS6KA3 Diagnosed by Exome Sequencing and a Literature Review.” Annals of Pediatric Endocrinology & Metabolism, vol. 28, no. 1, Mar. 2023, pp. 67–72. EBSCOhost, https://doi.org/10.6065/apem.2142134.067.
APA
Ari Song, Minji Im, Min-Sun Kim, Eu Seon Noh, Chiwoo Kim, Jahyun Jang, Sae-Mi Lee, Chang-Seok Ki, Sung Yoon Cho, & Dong-Kyu Jin. (2023). First female Korean child with Coffin-Lowry syndrome: a novel variant in RPS6KA3 diagnosed by exome sequencing and a literature review. Annals of Pediatric Endocrinology & Metabolism, 28(1), 67–72. https://doi.org/10.6065/apem.2142134.067
Chicago
Ari Song, Minji Im, Min-Sun Kim, Eu Seon Noh, Chiwoo Kim, Jahyun Jang, Sae-Mi Lee, Chang-Seok Ki, Sung Yoon Cho, and Dong-Kyu Jin. 2023. “First Female Korean Child with Coffin-Lowry Syndrome: A Novel Variant in RPS6KA3 Diagnosed by Exome Sequencing and a Literature Review.” Annals of Pediatric Endocrinology & Metabolism 28 (1): 67–72. doi:10.6065/apem.2142134.067.