<i>PEX26</i> gene genotype-phenotype correlation in neonates with Zellweger syndrome.

He, Yue; Lin, Sam Bill; Li, Wen-Xuan; Yang, Lin; Zhang, Rong; Chen, Chao; Yuan, Lin

PEX26 gene genotype-phenotype correlation in neonates with Zellweger syndrome.

He, Yue; Lin, Sam Bill; Li, Wen-Xuan; Yang, Lin; Zhang, Rong; Chen, Chao; Yuan, Lin.

Afiliação

He Y; Department of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Lin SB; Department of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Li WX; Department of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Yang L; Clinical Genetic Center, Children's Hospital of Fudan University, Shanghai, China.
Zhang R; Department of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Chen C; Department of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Yuan L; Department of Neonatology, Children's Hospital of Fudan University, Shanghai, China.

Transl Pediatr ; 10(7): 1825-1833, 2021 Jul.

Article em En | MEDLINE | ID: mdl-34430430

Palavras-chave

PEX26; Zellweger spectrum disorder (ZSD); Zellweger syndrome (ZS); newborn

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Systematic_reviews Idioma: En Revista: Transl Pediatr Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

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