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

1. Porriño-Bustamante, M.L.
2. López-Nevot, M.Á.
3. Aneiros-Fernández, J.
4. Casado-Ruiz, J.
5. García-Linares, S.
6. Pedrinacci-Rodríguez, S.
7. García-Lora, E.
8. Martín-Casares, M.A.
9. Fernández-Pugnaire, M.A.
10. Arias-Santiago, S.