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
FI: 1,701
Type: Article
Collaboration
Year: 2019
Writers
Porrino-Bustamante, ML; Lopez-Nevot, MA; Aneiros-Fernandez, J; Married-Ruiz, J; Garcia-Linares, S; Pedrinacci-Rodriguez, S; Garcia-Lora, E; Martin-Casares, MA; Fernandez-Pugnaire, MA; Arias-Santiago, S.
Magazine
Title: AUSTRALASIAN JOURNAL OF DERMATOLOGY
Quartile
- Q3