[Analysis of PROKR2 gene mutation in patients with hypogonadotropic hypogonadism].

Xie, Y D; Zheng, R Z; Han, H J; Yuan, J D; Li, Jiada

Xie, Y D; Zheng, R Z; Han, H J; Yuan, J D; Li, Jiada.

Afiliación

Xie YD; Department of Endocrinology, People's Hospital of Henan University (Henan Provincial People's Hospital), Zhengzhou 450003, China.
Zheng RZ; Department of Endocrinology, People's Hospital of Henan University (Henan Provincial People's Hospital), Zhengzhou 450003, China.
Han HJ; Department of Endocrinology, People's Hospital of Henan University (Henan Provincial People's Hospital), Zhengzhou 450003, China.
Yuan JD; Department of Endocrinology, People's Hospital of Henan University (Henan Provincial People's Hospital), Zhengzhou 450003, China.
Li J; Central South University Medical Genetics Research Center, Changsha 430074, China.

Zhonghua Nei Ke Za Zhi ; 61(8): 933-936, 2022 Aug 01.

Article en Zh | MEDLINE | ID: mdl-35922219

Asunto(s)

Hipogonadismo; Humanos; Hipogonadismo/genética; Mutación; Mutación Missense; Receptores Acoplados a Proteínas G/genética; Receptores de Péptidos/genética; Estudios Retrospectivos

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hipogonadismo Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: Zh Revista: Zhonghua Nei Ke Za Zhi Año: 2022 Tipo del documento: Article País de afiliación: China

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