A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma
LOR基因中一种新的微缺失导致常染色体显性遗传性角化病
期刊:British Journal of Dermatology
影响因子:9.6
doi:10.1111/bjd.13361
Kinsler, V A; Drury, S; Khan, A; Waelchli, R; Rukaite, G; Barnicoat, A; Lench, N; Harper, J I; O'Shaughnessy, R F L
