G. Zhang

Mutations in the mevalonate pathway genes in Chinese patients with porokeratosis

N. Wilson, F. Chen, X. Li, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

Identification of one Novel complex delins mutation and one recurrent mutation of ERCC8 gene in a Chinese family with Cockayne Syndrome A

U. Keyal, A. K. Bhatta, Y. Hua, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

Novel splice‐site and frameshift ATP2A2 mutations in Chinese patients with Darier disease

M. Li, H. Shi, H. Mu, 2012, Clincal and Experimental Dermatology.

Two novel ATP2C1 mutations in patients with Hailey-Hailey disease and a literature review of sequence variants reported in the Chinese population.

M. Shao, L. Zhang, Y. Gu, 2015, Genetics and molecular research : GMR.

Mutations in the ADAR1 gene in Chinese families with dyschromatosis symmetrica hereditaria.

M. Li, H. Shi, H. Mu, 2013, Genetics and molecular research : GMR.

Features and clinical significance of tertiary lymphoid structure in cutaneous squamous cell carcinoma

Y. Liu, S. Fang, Q. Zeng, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.