Siblings of neonatal hyperbilirubinemia with <i>UGT1A1</i> double missense variants.

Kubota, Yoshiki; Sato, Takeshi; Matsuyama, Mai; Maruo, Yoshihiro; Narumi, Satoshi; Ishii, Tomohiro; Hasegawa, Tomonobu

Siblings of neonatal hyperbilirubinemia with UGT1A1 double missense variants.

Kubota, Yoshiki; Sato, Takeshi; Matsuyama, Mai; Maruo, Yoshihiro; Narumi, Satoshi; Ishii, Tomohiro; Hasegawa, Tomonobu.

Afiliação

Kubota Y; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Sato T; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Matsuyama M; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Maruo Y; Department of Pediatrics, Shiga University of Medical Science, Shiga, Japan.
Narumi S; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Ishii T; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Hasegawa T; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.

Clin Pediatr Endocrinol ; 33(3): 195-198, 2024.

Article em En | MEDLINE | ID: mdl-38993722

Palavras-chave

UGT1A1; double; hyperbilirubinemia; missense variant; neonate

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Pediatr Endocrinol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão País de publicação: Japão

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