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DNA hypermethylation and X chromosome inactivation are major determinants of phenotypic variation in women heterozygous for G6PD mutations.
Wang, Jin; Xiao, Qi-Zhi; Chen, You-Ming; Yi, Sheng; Liu, Dun; Liu, Yan-Hui; Zhang, Cui-Mei; Wei, Xiao-Feng; Zhou, Yu-Qiu; Zhong, Xing-Ming; Zhao, Cun-You; Xiong, Fu; Wei, Xiang-Cai; Xu, Xiang-Min.
Afiliação
  • Wang J; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
  • Xiao QZ; Department of Birth Health and Heredity, Zhuhai Women and Children Care Hospital, Zhuhai, Guangdong, China.
  • Chen YM; Department of Clinical Laboratory, the Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong, China.
  • Yi S; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
  • Liu D; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
  • Liu YH; Prenatal Diagnosis Center, Dongguan Maternal and Child Health Hospital, Dongguan, Guangdong, China.
  • Zhang CM; Department of Child Health, Boai Hospital of Zhongshan, Zhongshan, Guangdong, China.
  • Wei XF; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
  • Zhou YQ; Department of Birth Health and Heredity, Zhuhai Women and Children Care Hospital, Zhuhai, Guangdong, China.
  • Zhong XM; Department of Reproductive Immunology and Endocrinology, Family Planning Research Institute of Guangdong, Guangzhou, Guangdong, China.
  • Zhao CY; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
  • Xiong F; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
  • Wei XC; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China; Department of Reproductive Immunology and Endocrinology, Family Planning Research Institute of Guangdong, Guangzhou, Guangdong, China.
  • Xu XM; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China. Electronic address: gzxuxm@pub.guangzhou.gd.cn.
Blood Cells Mol Dis ; 53(4): 241-5, 2014 Dec.
Article em En | MEDLINE | ID: mdl-24958328
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Metilação de DNA / Mutação de Sentido Incorreto / Inativação do Cromossomo X / Glucosefosfato Desidrogenase / Deficiência de Glucosefosfato Desidrogenase Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans Idioma: En Revista: Blood Cells Mol Dis Assunto da revista: HEMATOLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Metilação de DNA / Mutação de Sentido Incorreto / Inativação do Cromossomo X / Glucosefosfato Desidrogenase / Deficiência de Glucosefosfato Desidrogenase Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans Idioma: En Revista: Blood Cells Mol Dis Assunto da revista: HEMATOLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos