Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2.

Morikawa, Shuntaro; Komatsu, Nagisa; Sakata, Sonoko; Nakamura-Utsunomiya, Akari; Okada, Satoshi; Tajima, Toshihiro

Morikawa, Shuntaro; Komatsu, Nagisa; Sakata, Sonoko; Nakamura-Utsunomiya, Akari; Okada, Satoshi; Tajima, Toshihiro.

Afiliação

Morikawa S; Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan.
Komatsu N; Department of Pediatrics, Japanese Red Cross Hospital Kumamoto, Kumamoto, Japan.
Sakata S; Department of Pediatrics, Hiroshima University Graduate School of Biomedical & Health Sciences, Hiroshima, Japan.
Nakamura-Utsunomiya A; Department of Pediatrics, Hiroshima University Graduate School of Biomedical & Health Sciences, Hiroshima, Japan.
Okada S; Department of Pediatrics, Hiroshima University Graduate School of Biomedical & Health Sciences, Hiroshima, Japan.
Tajima T; Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan.

Clin Pediatr Endocrinol ; 24(3): 135-8, 2015 Jul.

Article em En | MEDLINE | ID: mdl-26594094

Palavras-chave

NR3C2; mutation; pseudohypoaldosteronism type 1 (PHA1)

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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Clin Pediatr Endocrinol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão

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