WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

Hyung Goo Kim, Jang Won Ahn, Ingo Kurth, Reinhard Ullmann, Hyun Taek Kim, Anita Kulharya, Kyung Soo Ha, Yasuhide Itokawa, Irene Meliciani, Wolfgang Wenzel, Deresa Lee, Georg Rosenberger, Metin Ozata, David P. Bick, Richard J. Sherins, Takahiro Nagase, Mustafa Tekin, Soo Hyun Kim, Cheol Hee Kim, Hans Hilger RopersJames F. Gusella, Vera Kalscheuer, Cheol Yong Choi, Lawrence C. Layman

Research output: Contribution to journal › Article › peer-review

147 Scopus citations

Fingerprint

Dive into the research topics of 'WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome'. Together they form a unique fingerprint.

Medicine & Life Sciences