The first Japanese case of central precocious puberty with a novel <i>MKRN3</i> mutation.

Nishioka, Junko; Shima, Hirohito; Fukami, Maki; Yatsuga, Shuichi; Matsumoto, Takako; Ushijima, Kikumi; Kitamura, Miyuki; Koga, Yasutoshi

The first Japanese case of central precocious puberty with a novel MKRN3 mutation.

Nishioka, Junko; Shima, Hirohito; Fukami, Maki; Yatsuga, Shuichi; Matsumoto, Takako; Ushijima, Kikumi; Kitamura, Miyuki; Koga, Yasutoshi.

Afiliação

Nishioka J; Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Shima H; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Fukami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Yatsuga S; Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Matsumoto T; Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Ushijima K; Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Kitamura M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Koga Y; Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.

Hum Genome Var ; 4: 17017, 2017.

Article em En | MEDLINE | ID: mdl-28546864

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hum Genome Var Ano de publicação: 2017 Tipo de documento: Article

Texto completo

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PubMed Links

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hum Genome Var Ano de publicação: 2017 Tipo de documento: Article