Your browser doesn't support javascript.
loading
Identification of a novel de novo GATA3 mutation in a patient with HDR syndrome.
Chen, Liu; Chen, Bing; Leng, Wuilin; Lui, Xiaotian; Wu, Qinan; Ouyang, Xinshou; Liang, Ziwen.
Afiliação
  • Chen L; Department of Endocrinology, First Affiliated Hospital of Third Military Medical University, Chongqing, China.
  • Chen B; Department of Endocrinology, First Affiliated Hospital of Third Military Medical University, Chongqing, China.
  • Leng W; Department of Endocrinology, First Affiliated Hospital of Third Military Medical University, Chongqing, China.
  • Lui X; Department of Endocrinology, First Affiliated Hospital of Third Military Medical University, Chongqing, China.
  • Wu Q; Department of Endocrinology, First Affiliated Hospital of Third Military Medical University, Chongqing, China.
  • Ouyang X; Section of Digestive Disease, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
  • Liang Z; Department of Endocrinology, First Affiliated Hospital of Third Military Medical University, Chongqing, China ziwenliang99@163.com.
J Int Med Res ; 43(5): 718-24, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26268891
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator de Transcrição GATA3 / Perda Auditiva Neurossensorial / Hipoparatireoidismo / Mutação / Nefrose Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator de Transcrição GATA3 / Perda Auditiva Neurossensorial / Hipoparatireoidismo / Mutação / Nefrose Idioma: En Ano de publicação: 2015 Tipo de documento: Article