1. Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria
   Lu Cao et al, 2021, BMC Medical Genomics CrossRef
2. The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
   Hongyu Chen et al, 2023, Journal of Molecular Medicine CrossRef
3. The emerging and diverse roles of the SLy/SASH1‐protein family in health and disease—Overview of three multifunctional proteins
   Jennifer Jaufmann et al, 2021, The FASEB Journal CrossRef
4. Retyping and molecular pathology diagnosis of dyschromatosis universalis hereditaria
   Ding'an Zhou et al, 2023, Experimental Dermatology CrossRef