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Characterization of Mutations Causing CYP21A2 Deficiency in Brazilian and Portuguese Populations.
Prado, Mayara J; Singh, Shripriya; Ligabue-Braun, Rodrigo; Meneghetti, Bruna V; Rispoli, Thaiane; Kopacek, Cristiane; Monteiro, Karina; Zaha, Arnaldo; Rossetti, Maria L R; Pandey, Amit V.
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  • Prado MJ; Graduate Program in Cell and Molecular Biology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre 91501-970, Brazil.
  • Singh S; Center for Biotechnology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre 91501-970, Brazil.
  • Ligabue-Braun R; Department of Biomedical Research, University of Bern, 3010 Bern, Switzerland.
  • Meneghetti BV; Pediatric Endocrinology Unit, Department of Pediatrics, University Children's Hospital Bern, 3010 Bern, Switzerland.
  • Rispoli T; Department of Biomedical Research, University of Bern, 3010 Bern, Switzerland.
  • Kopacek C; Pediatric Endocrinology Unit, Department of Pediatrics, University Children's Hospital Bern, 3010 Bern, Switzerland.
  • Monteiro K; Departament of Pharmacosciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre 90050-170, Brazil.
  • Zaha A; Graduate Program in Cell and Molecular Biology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre 91501-970, Brazil.
  • Rossetti MLR; Center for Biotechnology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre 91501-970, Brazil.
  • Pandey AV; Graduate Program in Cell and Molecular Biology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre 91501-970, Brazil.
Int J Mol Sci ; 23(1)2021 Dec 28.
Article en En | MEDLINE | ID: mdl-35008721
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esteroide 21-Hidroxilasa / Genética de Población / Mutación Tipo de estudio: Prognostic_studies Límite: Adolescent / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: America do sul / Brasil / Europa Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Brasil
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esteroide 21-Hidroxilasa / Genética de Población / Mutación Tipo de estudio: Prognostic_studies Límite: Adolescent / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: America do sul / Brasil / Europa Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Brasil