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Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency.
Zhang, Ya-Xin; He, Wen-Bin; Xiao, Wen-Juan; Meng, Lan-Lan; Tan, Chen; Du, Juan; Lu, Guang-Xiu; Lin, Ge; Tan, Yue-Qiu.
Afiliación
  • Zhang YX; Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, Hunan, PR China.
  • He WB; Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, Hunan, PR China.
  • Xiao WJ; Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, Hunan, PR China.
  • Meng LL; Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, Hunan, PR China.
  • Tan C; Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, Hunan, PR China.
  • Du J; Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, Hunan, PR China.
  • Lu GX; Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, Hunan, PR China.
  • Lin G; Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, Hunan, PR China.
  • Tan YQ; Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, Hunan, PR China.
Mol Genet Genomic Med ; 8(4): e1165, 2020 04.
Article en En | MEDLINE | ID: mdl-32048466
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Proteínas de Mantenimiento de Minicromosoma / Mutación con Pérdida de Función Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Proteínas de Mantenimiento de Minicromosoma / Mutación con Pérdida de Función Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos