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PITX2 loss-of-function mutation contributes to tetralogy of Fallot.
Sun, Yu-Min; Wang, Jun; Qiu, Xing-Biao; Yuan, Fang; Xu, Ying-Jia; Li, Ruo-Gu; Qu, Xin-Kai; Huang, Ri-Tai; Xue, Song; Yang, Yi-Qing.
Afiliação
  • Sun YM; Department of Cardiology, Jing'an District Central Hospital, 259 Xikang Road, Shanghai 200040, PR China.
  • Wang J; Department of Cardiology, Jing'an District Central Hospital, 259 Xikang Road, Shanghai 200040, PR China. Electronic address: wang_jun98@sina.cn.
  • Qiu XB; Department of Cardiology, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 West Huaihai Road, Shanghai 200030, PR China.
  • Yuan F; Department of Cardiology, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 West Huaihai Road, Shanghai 200030, PR China.
  • Xu YJ; Department of Cardiology, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 West Huaihai Road, Shanghai 200030, PR China.
  • Li RG; Department of Cardiology, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 West Huaihai Road, Shanghai 200030, PR China.
  • Qu XK; Department of Cardiology, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 West Huaihai Road, Shanghai 200030, PR China.
  • Huang RT; Department of Cardiovascular Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, 1630 Dongfang Road, Shanghai 200127, PR China.
  • Xue S; Department of Cardiovascular Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, 1630 Dongfang Road, Shanghai 200127, PR China.
  • Yang YQ; Department of Cardiology, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 West Huaihai Road, Shanghai 200030, PR China; Department of Cardiovascular Research Laboratory, Shanghai Chest Hospital, Shanghai Jiao Tong University, 241 West Huaihai Road, Shanghai 200030, PR China; Department o
Gene ; 577(2): 258-64, 2016 Feb 15.
Article em En | MEDLINE | ID: mdl-26657035
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles / 7_ODS3_muertes_prevenibles_nacidos_ninos Problema de saúde: 2_muertes_prevenibles / 6_cardiovascular_diseases / 6_congenital_chromosomal_anomalies / 6_other_circulatory_diseases / 7_neonatal_care_health / 7_non_communicable_diseases Assunto principal: Tetralogia de Fallot / Fatores de Transcrição / Proteínas de Homeodomínio / Mutação de Sentido Incorreto Tipo de estudo: Prognostic_studies Limite: Animals / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Gene Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles / 7_ODS3_muertes_prevenibles_nacidos_ninos Problema de saúde: 2_muertes_prevenibles / 6_cardiovascular_diseases / 6_congenital_chromosomal_anomalies / 6_other_circulatory_diseases / 7_neonatal_care_health / 7_non_communicable_diseases Assunto principal: Tetralogia de Fallot / Fatores de Transcrição / Proteínas de Homeodomínio / Mutação de Sentido Incorreto Tipo de estudo: Prognostic_studies Limite: Animals / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Gene Ano de publicação: 2016 Tipo de documento: Article