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Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review.
Sugisawa, Chiho; Taniyama, Matsuo; Sato, Takeshi; Takahashi, Yasuyoshi; Hasegawa, Tomonobu; Narumi, Satoshi.
Afiliação
  • Sugisawa C; Division of Diabetes, Metabolism and Endocrinology, Showa University Fujigaoka Hospital, Kanagawa 227-8501, Japan.
  • Taniyama M; Department of Pediatrics, Keio University School of Medicine, Tokyo 160-8582, Japan.
  • Sato T; Division of Diabetes, Metabolism and Endocrinology, Showa University Fujigaoka Hospital, Kanagawa 227-8501, Japan.
  • Takahashi Y; Division of Diabetes and Endocrinology, Department of Internal Medicine, Showa University School of Medicine, Tokyo 142-8555, Japan.
  • Hasegawa T; Department of Pediatrics, Keio University School of Medicine, Tokyo 160-8582, Japan.
  • Narumi S; Division of Diabetes and Endocrinology, Department of Internal Medicine, Showa University School of Medicine, Tokyo 142-8555, Japan.
Endocr J ; 69(7): 831-838, 2022 Jul 28.
Article em En | MEDLINE | ID: mdl-35236788
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Kallmann / Receptores de Peptídeos / Receptores Acoplados a Proteínas G / Diabetes Mellitus Tipo 2 / Hipogonadismo Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Kallmann / Receptores de Peptídeos / Receptores Acoplados a Proteínas G / Diabetes Mellitus Tipo 2 / Hipogonadismo Idioma: En Ano de publicação: 2022 Tipo de documento: Article