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Novel PMM2 missense mutation in a Chinese family with non-syndromic premature ovarian insufficiency.
Peng, Tianliu; Lv, Chao; Tan, Hangjing; Huang, Jiafeng; He, Hailun; Wang, Yan; Zeng, Minghua; Yi, Dajing; Li, Jie; Deng, Hongwen; Shi, Xiaobo; Xiao, Hongmei.
  • Peng T; Institute of Reproductive & Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, 410013, China.
  • Lv C; Center for Reproductive Health and Systems Biology and Data information, School of Basic Medical Science, Central South University, Changsha, 410013, Hunan, China.
  • Tan H; Institute of Reproductive & Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, 410013, China.
  • Huang J; Center for Reproductive Health and Systems Biology and Data information, School of Basic Medical Science, Central South University, Changsha, 410013, Hunan, China.
  • He H; Institute of Reproductive & Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, 410013, China.
  • Wang Y; Center for Reproductive Health and Systems Biology and Data information, School of Basic Medical Science, Central South University, Changsha, 410013, Hunan, China.
  • Zeng M; Life of Sciences, Central South University, Changsha, 410013, China.
  • Yi D; Life of Sciences, Central South University, Changsha, 410013, China.
  • Li J; Institute of Reproductive & Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, 410013, China.
  • Deng H; Center for Reproductive Health and Systems Biology and Data information, School of Basic Medical Science, Central South University, Changsha, 410013, Hunan, China.
  • Shi X; Institute of Reproductive & Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, 410013, China.
  • Xiao H; Center for Reproductive Health and Systems Biology and Data information, School of Basic Medical Science, Central South University, Changsha, 410013, Hunan, China.
J Assist Reprod Genet ; 37(2): 443-450, 2020 Feb.
Article en En | MEDLINE | ID: mdl-31902100
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Fosfotransferasas (Fosfomutasas) / Predisposición Genética a la Enfermedad Límite: Adult / Female / Humans País como asunto: Asia Idioma: En Año: 2020 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Fosfotransferasas (Fosfomutasas) / Predisposición Genética a la Enfermedad Límite: Adult / Female / Humans País como asunto: Asia Idioma: En Año: 2020 Tipo del documento: Article