Variant predictions in congenital adrenal hyperplasia caused by mutations in CYP21A2.

Prado, Mayara J; Ligabue-Braun, Rodrigo; Zaha, Arnaldo; Rossetti, Maria Lucia Rosa; Pandey, Amit V

Prado, Mayara J; Ligabue-Braun, Rodrigo; Zaha, Arnaldo; Rossetti, Maria Lucia Rosa; Pandey, Amit V.

Afiliación

Prado MJ; Graduate Program in Cell and Molecular Biology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil.
Ligabue-Braun R; Center for Biotechnology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil.
Zaha A; Translational Hormone Research, Department of Biomedical Research, University of Bern, Bern, Switzerland.
Rossetti MLR; Pediatric Endocrinology Unit, Department of Pediatrics, University Children's Hospital Bern, Bern, Switzerland.
Pandey AV; Departament of Pharmacosciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.

Front Pharmacol ; 13: 931089, 2022.

Article en En | MEDLINE | ID: mdl-36278220

Palabras clave

CAH; CYP21A2; mutation analysis; online prediction; pathogenicity prediction tools; steroid metabolism

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Pharmacol Año: 2022 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Suiza

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