Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency

por Mo, Eun Yeong, Lee, Ji-young, Kim, Su Yeon, Kim, Min Ji, Kim, Eun Sook, Lee, Seungok, Han, Je Ho, Moon, Sung-dae
Publicado 2018

Clinical features and signaling effects of RET D631Y variant multiple endocrine neoplasia type 2 (MEN2)

por Lee, Ji-young, Kim, Su Yeon, Jo, Kwan Hoon, Mo, Eun Yeong, Kim, Eun Sook, Kim, Hye Soo, Han, Je Ho, Moon, Sung-dae
Publicado 2022