Hu, L., Chen, L., Yang, L., Ye, Z., Huang, W., Li, X., . . . Ding, X. (2020). KCTD1 mutants in scalp-ear-nipple syndrome and AP-2α P59A in Char syndrome reciprocally abrogate their interactions, but can regulate Wnt/β-catenin signaling. Mol Med Rep.

Hu, Lingyu, Li Chen, Liu Yang, Zi Ye, Wenhuan Huang, Xinxin Li, Qing Liu, Junlu Qiu, e Xiaofeng Ding. "KCTD1 Mutants in Scalp-ear-nipple Syndrome and AP-2α P59A in Char Syndrome Reciprocally Abrogate Their Interactions, but Can Regulate Wnt/β-catenin Signaling." Mol Med Rep 2020.

Hu, Lingyu, et al. "KCTD1 Mutants in Scalp-ear-nipple Syndrome and AP-2α P59A in Char Syndrome Reciprocally Abrogate Their Interactions, but Can Regulate Wnt/β-catenin Signaling." Mol Med Rep 2020.