Novel WEE2 homozygous mutations c.1346C>T and c.949A>T identified in primary infertile women due to unexplained fertilization failure.

Guo, Haiyan; Wu, Haibo; Yan, Zheng; Yin, Mingru; Wu, Ling; Li, Bin

Guo, Haiyan; Wu, Haibo; Yan, Zheng; Yin, Mingru; Wu, Ling; Li, Bin.

Afiliación

Guo H; Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Wu H; Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yan Z; Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yin M; Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Wu L; Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Li B; Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Clin Genet ; 104(6): 700-704, 2023 12.

Article en En | MEDLINE | ID: mdl-37772619

Asunto(s)

Infertilidad Femenina; Femenino; Humanos; Fertilización; Fertilización In Vitro; Infertilidad Femenina/genética; Mutación; Mutación Missense; Insuficiencia del Tratamiento

Palabras clave

TFF; WEE2; fertilization failure; mutation

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infertilidad Femenina Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Clin Genet Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Dinamarca

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