Study of Human Leukocyte Antigen (HLA) in 13 cases of familial frontal fibrosing alopecia: CYP21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA-A*33:01; B*14:02; C*08:02 as a genetic marker

Colaboración

Año: 2019

Porrino-Bustamante, ML; Lopez-Nevot, MA; Aneiros-Fernandez, J; Casado-Ruiz, J; Garcia-Linares, S; Pedrinacci-Rodriguez, S; Garcia-Lora, E; Martin-Casares, MA; Fernandez-Pugnaire, MA; Arias-Santiago, S

Título: AUSTRALASIAN JOURNAL OF DERMATOLOGY

• Q3