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Primary ciliary dyskinesia due to CCNO mutations-A genotype-phenotype correlation contribution.
Henriques, Ana Raquel; Constant, Carolina; Descalço, Andreia; Pinto, Andreia; Moura Nunes, J; Sampaio, Pedro; Lopes, Susana S; Pereira, Luísa; Bandeira, Teresa.
Afiliação
  • Henriques AR; Department of Paediatrics, Hospital de Santa Maria-Centro Hospitalar Universitário de Lisboa Norte, Lisbon, Portugal.
  • Constant C; Paediatric Respiratory Unit, Department of Paediatrics, Hospital de Santa Maria-Centro Hospitalar Universitário de Lisboa Norte, Lisbon, Portugal.
  • Descalço A; Paediatric Lung Function Laboratory, Department of Paediatrics, Hospital de Santa Maria-Centro Hospitalar Universitário de Lisboa Norte, Lisbon, Portugal.
  • Pinto A; Lisbon Academic Medical Centre, University of Lisbon, Lisbon, Portugal.
  • Moura Nunes J; Paediatric Lung Function Laboratory, Department of Paediatrics, Hospital de Santa Maria-Centro Hospitalar Universitário de Lisboa Norte, Lisbon, Portugal.
  • Sampaio P; Histology and Comparative Pathology Unit, Institute of Molecular Medicine João Lobo Antunes, Lisbon Academic Medical Centre, University of Lisbon, Lisbon, Portugal.
  • Lopes SS; Portuguese Institute of Oncology Francisco Gentil, Lisbon, Portugal.
  • Pereira L; Cilia Regulation and Disease Lab, iNOVA4HEALTH, CEDOC, NOVA Medical School, Nova University of Lisbon, Lisbon, Portugal.
  • Bandeira T; Cilia Regulation and Disease Lab, iNOVA4HEALTH, CEDOC, NOVA Medical School, Nova University of Lisbon, Lisbon, Portugal.
Pediatr Pulmonol ; 56(8): 2776-2779, 2021 08.
Article em En | MEDLINE | ID: mdl-34102041

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Kartagener / Transtornos da Motilidade Ciliar / DNA Glicosilases Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Kartagener / Transtornos da Motilidade Ciliar / DNA Glicosilases Idioma: En Ano de publicação: 2021 Tipo de documento: Article