Primary ciliary dyskinesia due to CCNO mutations : a genotype‐phenotype correlation contribution

© 2021 Wiley Periodicals LLC

Detalhes bibliográficos
Autor principal: Henriques, Ana Raquel (author)
Outros Autores: Constant, Carolina (author), Descalço, Andreia (author), Pinto, Andreia (author), Moura Nunes, J. (author), Sampaio, Pedro (author), Lopes, Susana S. (author), Pereira, Luísa (author), Bandeira, Teresa (author)
Formato: article
Idioma:eng
Publicado em: 2021
Assuntos:
CCNO mutations
Child
Chronic diseases
Ciliary motility disorders
Texto completo:http://hdl.handle.net/10451/48683
País:Portugal
Oai:oai:repositorio.ul.pt:10451/48683

Texto Completo

http://hdl.handle.net/10451/48683

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