Associated Papers
Novel Insights into the Enigmatic Genetics of Male Breast Cancer in China.
Lang GT et al.
Pathophysiology : the Official Journal of the International Society for Pathophysiology, 2026
41718387 (PubMed )
Supplement: pathophysiology-33-00009-s001.zip › Supplementary_Table_1.pdf
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project.
Cong PK et al.
Nature Communications, 2022
35618720 (PubMed )
Supplement: 41467_2022_30526_MOESM5_ESM.xlsx › Data_2
A novel oncostatin M/interleukin-31 receptor mutation in familial primary localized cutaneous amyloidosis.
Adams R et al.
Clinical and Experimental Dermatology, 2020
Clinical and genetic features of Chinese patients with lichen and macular primary localized cutaneous amyloidosis.
Lu P et al.
Clinical and Experimental Dermatology, 2019
Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis.
Qiu YL et al.
Hepatology (baltimore, Md.), 2017
28027573 (PubMed )
Supplement: HEP-65-1655-s001.pdf
The molecular skin pathology of familial primary localized cutaneous amyloidosis.
Tanaka A et al.
Experimental Dermatology, 2010
Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis.
Lin MW et al.
European Journal of Human Genetics : Ejhg, 2010
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