J. Ji

T helper 22 cells from Han Chinese patients with atopic dermatitis exhibit high expression of inducible T‐cell costimulator

M. Maurer, Q. Qian, Q. Jiao, 2020, The British journal of dermatology.

Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos disease.

F. Hao, Heng Yan, Ming Li, 2013, American journal of human genetics.

Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria

Guolong Zhang, Z. Yao, M. Lai, 2010, Archives of Dermatological Research.

Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.

D. Choo, Ronghua Li, Yaping Qian, 2006, Biochemical and biophysical research communications.

Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract

X. Tang, X. Yuan, Z. Ma, 2005, British Journal of Ophthalmology.