المؤلفون: Kim, Soo Y., Lee, Seungbok, Woo, Hyewon, Han, Jiyeon, Ko, Young J., Shim, Youngkyu, Park, Soojin, Jang, Se S., Lim, Byung C., Ko, Jung M., Kim, Ki J., Cho, Anna, Kim, Hunmin, Hwang, Hee, Choi, Ji E., Kim, Man J., Moon, Jangsup, Seong, Moon-Woo, Park, Sung S., Choi, Sun A., Lee, Ji E., Kwon, Young S., Sohn, Young B., Kim, Jon S., Kim, Won S., Lee, Yun J., Kwon, Soonhak, Kim, Young O., Kook, Hoon, Cho, Yong G., Cheon, Chong K., Kang, Ki-Soo, Song, Mi-Ryoung, Kim, Young-Joon, Cha, Hyuk-Jin, Choi, Hee-Jung, Kee, Yun, Park, Sung-Gyoo, Baek, Seung T., Choi, Murim, Ryu, Dong-Sung, Chae, Jong-Hee

Relation: Orphanet Journal of Rare Diseases. 2022 Oct 08;17(1):372; https://doi.org/10.1186/s13023-022-02520-5; https://hdl.handle.net/10371/186068

الاتاحة: https://hdl.handle.net/10371/186068
https://doi.org/10.1186/s13023-022-02520-5