[Primary ciliary dyskinesia caused by mutation of CCNO29 gene in a family report].

Sun, X P; Xu, J X; Wu, S Z; Zhu, H Y; Liu, H; Liu, Z Y; Yang, S; Lu, C Y; Chen, D H

Sun, X P; Xu, J X; Wu, S Z; Zhu, H Y; Liu, H; Liu, Z Y; Yang, S; Lu, C Y; Chen, D H.

Afiliação

Sun XP; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Xu JX; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Wu SZ; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Zhu HY; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Liu H; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Liu ZY; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Yang S; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Lu CY; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Chen DH; Department of Pediatrics, First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.

Zhonghua Er Ke Za Zhi ; 62(4): 378-380, 2024 Mar 25.

Article em Zh | MEDLINE | ID: mdl-38527512

Assuntos

Síndrome de Kartagener; Humanos; Síndrome de Kartagener/genética; Mutação; Cílios

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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome de Kartagener Limite: Humans Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

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