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Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II.
Wang, Xue-Ping; Hao, Zi-Qi; Liu, Ya-Lan; Mei, Ling-Yun; He, Chu-Feng; Niu, Zhi-Jie; Sun, Jie; Zhao, Yu-Lin; Feng, Yong.
Afiliação
  • Wang XP; Department of Otolaryngology Head and Neck Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
  • Hao ZQ; Central Laboratory of Taiyuan Hospital Center, Taiyuan, Shanxin, People's Republic of China.
  • Liu YL; Province Key Laboratory of Otolaryngology Critical Disease, Xiangya Hosipital, Central South University, Changsha, Hunan, People's Republic of China.
  • Mei LY; Department of Otolaryngology Head and Neck Surgery, Xiangya Hosipital, Central South University, Changsha, Hunan, People's Republic of China; Province Key Laboratory of Otolaryngology Critical Disease, Xiangya Hosipital, Central South University, Changsha, Hunan, People's Republic of China.
  • He CF; Department of Otolaryngology Head and Neck Surgery, Xiangya Hosipital, Central South University, Changsha, Hunan, People's Republic of China; Province Key Laboratory of Otolaryngology Critical Disease, Xiangya Hosipital, Central South University, Changsha, Hunan, People's Republic of China.
  • Niu ZJ; Department of Otolaryngology Head and Neck Surgery, Xiangya Hosipital, Central South University, Changsha, Hunan, People's Republic of China.
  • Sun J; Department of Otolaryngology, First Affiliated Hospital, Xinjiang Medical University, Urumqi, People's Republic of China.
  • Zhao YL; Department of Otolaryngology Head and Neck Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
  • Feng Y; Department of Otolaryngology Head and Neck Surgery, Xiangya Hosipital, Central South University, Changsha, Hunan, People's Republic of China; Province Key Laboratory of Otolaryngology Critical Disease, Xiangya Hosipital, Central South University, Changsha, Hunan, People's Republic of China; State Ke
Biochem Biophys Res Commun ; 493(1): 258-262, 2017 11 04.
Article em En | MEDLINE | ID: mdl-28893539
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Waardenburg / Haplótipos / Polimorfismo de Nucleotídeo Único / Fatores de Transcrição SOXE / Fator de Transcrição PAX3 Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Waardenburg / Haplótipos / Polimorfismo de Nucleotídeo Único / Fatores de Transcrição SOXE / Fator de Transcrição PAX3 Idioma: En Ano de publicação: 2017 Tipo de documento: Article