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Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous CA2 deletion.
Leite, Luan Deives Rodrigues; Resende, Kêmelly Karolliny Moreira; Rosa, Lídia Dos Santos; Mazzeu, Juliana Forte; de Oliveira, Livia Claudio; Scher, Maria do Carmo Sorci Dias; Acevedo, Ana Carolina; Yamaguti, Paulo Marcio.
Afiliación
  • Leite LDR; Oral Care Center for Inherited Diseases, Unit of Oral Health, University Hospital of Brasilia, University of Brasilia, Brasilia, Brazil.
  • Resende KKM; Oral Care Center for Inherited Diseases, Unit of Oral Health, University Hospital of Brasilia, University of Brasilia, Brasilia, Brazil.
  • Rosa LDS; Laboratory of Oral Histopathology, Department of Dentistry, Faculty of Health Sciences, University of Brasilia, Brasilia, Brazil.
  • Mazzeu JF; Laboratory of Clinical Genetics, Faculty of Medicine, University of Brasilia, Brasilia, Brazil.
  • de Oliveira LC; Unit of Pediatric Nephrology, University Hospital of Brasilia, University of Brasilia, Brasilia, Brazil.
  • Scher MDCSD; Unit of Pediatric Nephrology, University Hospital of Brasilia, University of Brasilia, Brasilia, Brazil.
  • Acevedo AC; Laboratory of Oral Histopathology, Department of Dentistry, Faculty of Health Sciences, University of Brasilia, Brasilia, Brazil.
  • Yamaguti PM; Oral Care Center for Inherited Diseases, Unit of Oral Health, University Hospital of Brasilia, University of Brasilia, Brasilia, Brazil.
Intractable Rare Dis Res ; 12(3): 202-205, 2023 Aug.
Article en En | MEDLINE | ID: mdl-37662627
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Intractable Rare Dis Res Año: 2023 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Japón
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Intractable Rare Dis Res Año: 2023 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Japón