Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Alopecia and CYP21A2[original query] |
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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. The Australasian journal of dermatology 2019 Jan . Porriño-Bustamante María Librada, López-Nevot Miguel Ángel, Aneiros-Fernández José, Casado-Ruiz Jorge, García-Linares Susana, Pedrinacci-Rodríguez Susana, García-Lora Elena, Martín-Casares María Antonia, Fernández-Pugnaire María Antonia, Arias-Santiago Salvad |
Non-Classical Congenital Adrenal Hyperplasia-Causing Alleles in Adolescent Girls with PCOS and in Risk Group for PCOS Development. Diagnostics (Basel, Switzerland) 2021 6 11 (6): . Lidaka Lasma, Bekere Laine, Lazdane Gunta, Dzivite-Krisane Iveta, Kivite-Urtane Anda, Gailite Lin |
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- Page last updated:Apr 22, 2024
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